GIST tumors arise from interstitial cells of Cajal in the gastrointestinal tract. They are typically positive for CD117 and CD34 markers. The majority of GISTs have mutations in genes like KIT or PDGFRA. Treatment involves surgical resection, though imatinib therapy can be used for advanced cases. Prognosis depends on factors like tumor size, mitotic rate, and location within the GI tract.
(1) Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the GI tract and arise from interstitial cells of Cajal. (2) Most GISTs involve the stomach and small intestine. (3) Clinical features vary depending on the size and location of the tumor, ranging from asymptomatic small tumors to abdominal pain, bleeding, or obstruction with larger tumors. (4) Surgery with clear margins remains the main treatment for localized GISTs, while targeted therapy with imatinib is recommended for advanced or metastatic disease.
This case report describes a 52-year-old male farmer who presented with abdominal pain and bleeding for several months. Imaging revealed multiple liver abscesses and a mass arising from the second part of the duodenum. Biopsy of the mass during endoscopy indicated adenocarcinoma. The patient underwent a Whipple procedure where a 6x5cm mass was removed. Post-operative biopsy found it to be a malignant gastrointestinal stromal tumor (GIST). The patient was referred for chemotherapy. GISTs of the duodenum are rare but often diagnosed via endoscopy with biopsy. Surgical resection is the main treatment but imatinib may help downstage tumors for less invasive surgery or as adjuvant therapy.
This document provides an outline and overview of gastrointestinal stromal tumors (GISTs). Some key points:
- GISTs are rare cancers that arise from interstitial cells of Cajal in the gastrointestinal tract. Most common in stomach and small intestine.
- Majority have activating mutations in KIT or PDGFRA genes leading to uncontrolled cell growth. 5% are hereditary syndromes.
- Diagnosis involves imaging (CT/MRI), endoscopy with biopsy for immunohistochemistry and genetic testing.
- Prognosis depends on tumor size, location, mitotic rate and genotype. Surgery is the main treatment, while tyrosine kinase inhibitors like imatininb are also
This document discusses the utility of integrating molecular genetics with soft tissue pathology. Key points include:
1) Molecular genetics can help more accurately define disease entities, improve diagnostic accuracy, and identify prognostic and therapeutic targets.
2) Techniques like FISH and PCR are useful for distinguishing subtypes of sarcomas and supporting diagnoses, especially in non-canonical cases.
3) Specific gene fusions and mutations have been identified that are diagnostic for entities like Ewing sarcoma, synovial sarcoma, and GIST.
4) While molecular findings cannot replace morphology, genetics provides an important adjunct for diagnosis, especially in challenging cases. The integration of both disciplines has enhanced understanding and classification of soft
Gastrointestinal stromal tumor (GIST) dr ridu kumar sharmaRidu Kumar Sharma
GISTs are the most common mesenchymal tumors of the GI tract. They are driven by mutations in c-Kit and PDGFR genes. Surgery is the main treatment for localized disease, while imatinib is effective systemic therapy for advanced or metastatic GISTs. Imatinib targets the c-Kit mutation to inhibit tumor growth with acceptable toxicity. Tumor size and mitotic index are prognostic factors used for risk stratification. Ongoing research is exploring additional targeted therapies to treat GISTs.
Gastrointerstinal stromal tumor (GIST) recent advances and differential diagn...Indira Shastry
This document provides information on gastrointestinal stromal tumors (GISTs), including:
- GISTs arise from interstitial cells of Cajal in the gastrointestinal tract and are defined by activating mutations in KIT or PDGFRA.
- Common symptoms are nonspecific but most GISTs are found in the stomach.
- Immunohistochemistry shows positivity for CD117 in 95% of cases, as well as DOG1, CD34, and protein kinase C theta.
- Risk stratification systems exist to determine malignant potential and guide treatment, which frequently involves tyrosine kinase inhibitors.
GIST tumors arise from interstitial cells of Cajal in the gastrointestinal tract. They are typically positive for CD117 and CD34 markers. The majority of GISTs have mutations in genes like KIT or PDGFRA. Treatment involves surgical resection, though imatinib therapy can be used for advanced cases. Prognosis depends on factors like tumor size, mitotic rate, and location within the GI tract.
(1) Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the GI tract and arise from interstitial cells of Cajal. (2) Most GISTs involve the stomach and small intestine. (3) Clinical features vary depending on the size and location of the tumor, ranging from asymptomatic small tumors to abdominal pain, bleeding, or obstruction with larger tumors. (4) Surgery with clear margins remains the main treatment for localized GISTs, while targeted therapy with imatinib is recommended for advanced or metastatic disease.
This case report describes a 52-year-old male farmer who presented with abdominal pain and bleeding for several months. Imaging revealed multiple liver abscesses and a mass arising from the second part of the duodenum. Biopsy of the mass during endoscopy indicated adenocarcinoma. The patient underwent a Whipple procedure where a 6x5cm mass was removed. Post-operative biopsy found it to be a malignant gastrointestinal stromal tumor (GIST). The patient was referred for chemotherapy. GISTs of the duodenum are rare but often diagnosed via endoscopy with biopsy. Surgical resection is the main treatment but imatinib may help downstage tumors for less invasive surgery or as adjuvant therapy.
This document provides an outline and overview of gastrointestinal stromal tumors (GISTs). Some key points:
- GISTs are rare cancers that arise from interstitial cells of Cajal in the gastrointestinal tract. Most common in stomach and small intestine.
- Majority have activating mutations in KIT or PDGFRA genes leading to uncontrolled cell growth. 5% are hereditary syndromes.
- Diagnosis involves imaging (CT/MRI), endoscopy with biopsy for immunohistochemistry and genetic testing.
- Prognosis depends on tumor size, location, mitotic rate and genotype. Surgery is the main treatment, while tyrosine kinase inhibitors like imatininb are also
This document discusses the utility of integrating molecular genetics with soft tissue pathology. Key points include:
1) Molecular genetics can help more accurately define disease entities, improve diagnostic accuracy, and identify prognostic and therapeutic targets.
2) Techniques like FISH and PCR are useful for distinguishing subtypes of sarcomas and supporting diagnoses, especially in non-canonical cases.
3) Specific gene fusions and mutations have been identified that are diagnostic for entities like Ewing sarcoma, synovial sarcoma, and GIST.
4) While molecular findings cannot replace morphology, genetics provides an important adjunct for diagnosis, especially in challenging cases. The integration of both disciplines has enhanced understanding and classification of soft
Gastrointestinal stromal tumor (GIST) dr ridu kumar sharmaRidu Kumar Sharma
GISTs are the most common mesenchymal tumors of the GI tract. They are driven by mutations in c-Kit and PDGFR genes. Surgery is the main treatment for localized disease, while imatinib is effective systemic therapy for advanced or metastatic GISTs. Imatinib targets the c-Kit mutation to inhibit tumor growth with acceptable toxicity. Tumor size and mitotic index are prognostic factors used for risk stratification. Ongoing research is exploring additional targeted therapies to treat GISTs.
Gastrointerstinal stromal tumor (GIST) recent advances and differential diagn...Indira Shastry
This document provides information on gastrointestinal stromal tumors (GISTs), including:
- GISTs arise from interstitial cells of Cajal in the gastrointestinal tract and are defined by activating mutations in KIT or PDGFRA.
- Common symptoms are nonspecific but most GISTs are found in the stomach.
- Immunohistochemistry shows positivity for CD117 in 95% of cases, as well as DOG1, CD34, and protein kinase C theta.
- Risk stratification systems exist to determine malignant potential and guide treatment, which frequently involves tyrosine kinase inhibitors.
Merkel Cell Carcinoma: From Diagnosis to Treatment (webinar)Natalie Richardson
This document provides an overview of Merkel cell carcinoma, including its histogenesis, pathogenesis, epidemiology, clinical features, diagnosis, staging, treatment options for both localized and metastatic disease, and prognosis. Key points discussed are the role of Merkel cell polyomavirus in pathogenesis, increasing incidence with age and sun exposure, diagnosis through biopsy and immunohistochemistry, standard treatment involving surgery and/or radiation for localized disease and chemotherapy or immunotherapy for advanced stages, and generally poor prognosis especially for metastatic or recurrent disease.
Circumcision early in life protects against carcinoma of the penis by reducing risk of HPV infection and preventing accumulation of smegma. Approximately half of penile carcinomas are HPV-related, with HPV-16 and HPV-18 being the most common types. Symptoms of penile carcinoma include masses, pain, bleeding, groin masses, and urinary symptoms. Diagnosis involves history, physical exam, biopsy, and imaging of lymph nodes. Staging uses the Jackson system or AJCC TNM system, with most cases being well-differentiated squamous cell carcinoma.
A 50-year-old woman presented with abdominal pain, a feeling of masses in her abdomen, and weight loss for three months. Clinical examination revealed two palpable abdominal masses. CT imaging showed multiple masses in the stomach and liver. Differentials included multicentric GIST, adenocarcinoma, and metastasis. Features pointed towards a diagnosis of multicentric GIST with liver metastasis, including the patient's age, well-defined heterogeneous stomach lesions, no lymphadenopathy or calcification, and absence of features against gastric adenocarcinoma.
This document summarizes a case series of 4 patients whose breast cancers were initially misdiagnosed as ductal carcinoma in situ (DCIS) but were later found to be invasive ductal carcinoma based on immunohistochemistry and lymph node involvement. In these cases, the cancers had a morphology that closely mimicked DCIS with central necrosis (comedo-type DCIS) but lacked a myoepithelial cell layer. Immunostains for myoepithelial markers were needed to correctly diagnose the cancers as invasive rather than DCIS and guide appropriate treatment. This case series highlights the importance of confirming DCIS diagnoses with immunohistochemistry to avoid misdiagnosing invasive breast cancers as non-invasive DCIS.
Gastrointestinal stromal tumors (GISTs) are rare mesenchymal tumors that arise from interstitial cells of Cajal in the gastrointestinal tract. GISTs most commonly present in the stomach and small intestine in patients in their late 60s, and median size is 5 cm. While small GISTs are often asymptomatic, larger tumors can cause vague symptoms like abdominal pain or bleeding. Diagnosis involves biopsy or excision of nodules over 2 cm. Immunohistochemistry shows 95% of GISTs are positive for CD117. Prognosis depends on tumor size, mitotic rate, and location. Treatment involves surgery for resectable localized disease and imatinib for advanced or metastatic
A 36-year-old male presented with a single grand mal seizure. MRI showed a well-defined hypodense mass in the left frontal lobe without enhancement or edema. Biopsy revealed a mixed grade II-III diffuse astrocytoma. Diffuse astrocytomas typically present as low-grade tumors that infiltrate the brain without symptoms. They have a tendency to transform into higher grades over time. Radiologically, they appear as well-defined lesions without enhancement or edema. The diagnosis in this case was a mixed grade II-III diffuse astrocytoma based on the MRI and biopsy findings.
Cancer is caused by defects in cell division that result from genetic mutations. Normal cell growth becomes unregulated, as cells multiply uncontrollably and crowd out healthy tissue. If cancer cells invade surrounding areas or spread to other parts of the body through metastasis and angiogenesis, it is considered malignant. Staging and grading of tumors helps determine prognosis and appropriate treatment options like surgery, radiation, chemotherapy, or targeted therapies.
This document contains medical information about a 55-year-old male patient presenting with a 1-year history of an ulcer on his penis, as well as swelling and pain in his groin region and scrotum over the past 8-6 months. Physical examination revealed the penile and groin ulcers, as well as swollen lymph nodes and scrotal enlargement. Biopsy of the penile ulcer showed well-differentiated squamous cell carcinoma. Imaging and tests identified secondary infection with Pseudomonas bacteria and scrotal elephantiasis. The patient was diagnosed with advanced penile cancer complicated by infection and elephantiasis, requiring total penectomy and lymph node dissection for treatment.
Gastrointestinal stromal tumors (GISTs) are rare sarcomas that arise from the gastrointestinal tract. Most commonly found in the stomach, they represent 0.2% of gastrointestinal tumors. While often asymptomatic, they can present with bleeding, pain, or obstruction. Diagnosis involves imaging such as endoscopy or CT scan followed by biopsy showing immunohistochemistry positive for CD117 in 95% of cases. Treatment involves surgical resection with clear margins although adjuvant therapy with imatinib is often used for higher risk tumors. Outcomes have improved greatly in the past two decades with 5-year survival rates now over 50% with appropriate treatment.
1) Ewing's sarcoma is a high-grade malignant bone tumor that most commonly affects children and young adults between 5-30 years old. It arises from bone marrow stem cells and is characterized by small, undifferentiated tumor cells and the translocation mutation t(11;22).
2) Clinically, patients present with pain, swelling, fever, and weight loss near the tumor site. Radiologically, the tumor appears osteolytic and aggressive, often with periosteal reaction. Histologically, it shows small, blue round cells with minimal cytoplasm and rosette formations.
3) Treatment involves chemotherapy, surgery, and radiation therapy. Prognosis is better with localized disease in children and
An MRI scan showed a large heterogeneously enhancing mass lesion in the right frontal region that crossed over to the left frontal region through the corpus callosum, causing mass effect on the lateral ventricles. Features were consistent with glioblastoma multiforme involving both frontal lobes. Glioblastoma multiforme is the most common and most aggressive form of brain cancer, typically occurring in adults between 45-60 years old. Treatment may include surgery, radiation therapy, chemotherapy and experimental therapies, but the cancer often recurs and median survival is less than one year.
This case report describes an 84-year old female patient with a neuroendocrine carcinoma of the breast diagnosed by fine needle aspiration cytology. The smears showed discohesive polygonal cells with abundant cytoplasm and eosinophilic granules. Histology confirmed a solid type neuroendocrine carcinoma with metastasis to lymph nodes. Immunohistochemistry was positive for markers like chromogranin and synaptophysin. Neuroendocrine carcinomas are rare breast tumors that can be diagnosed on cytology by observing characteristic cytoplasmic granules, though they may otherwise appear as invasive ductal carcinoma. Recognition of this rare tumor is important for prognosis and management.
The document discusses carcinoma penis, including its epidemiology, risk factors, pathology, staging, investigations, and treatment options. Premalignant lesions like erythroplasia of Queyrat and balanitis xerotica obliterans are described. Treatment depends on the stage and includes circumcision for small tumors, local excision, glansectomy, Mohs micrographic surgery, and laser surgery to preserve the organ while wide local excision or penectomy may be needed for more advanced cases.
History of DICER1 mutation
DICER1 function
Mutated DICER1 – tumorigenic mechanism
Constellation of lesions associated with DICER1
DICER1 IHC
When to test?
Therapeutic options
The document summarizes updates to the WHO 2020 classification of bone tumors. Key points include:
- Chondroblastoma is now classified as a benign tumor rather than intermediate based on its low metastasis rate.
- 95% of chondroblastomas harbor H3F3A or H3F3B mutations.
- Atypical cartilaginous tumor replaces chondrosarcoma in the appendicular skeleton to reflect variable prognosis between sites.
- Mesenchymal chondrosarcoma is defined by HEY1-NCOA2 fusions in over 90% of cases.
- Osteoblastoma and osteoid osteoma frequently demonstrate FOS/FOSB f
The document discusses recent updates in the diagnosis and grading of prostatic carcinoma, including revisions to Gleason scoring guidelines regarding lesions like cribriform and intraductal carcinoma. It also reviews the role of immunohistochemistry and molecular markers in prognostication as well as emerging applications of artificial intelligence in prostate cancer diagnosis.
Primitive neuroectodermal tumor (PNET) is a highly malignant tumor composed of small round cells of neuroectodermal origin that affects soft tissue and bone. PNETs are classified into groups depending on location, with peripheral PNET (pPNET) occurring in soft tissue and bone outside the central nervous system. pPNET includes Ewing sarcoma and Askin tumor. Diagnosis involves ruling out other small round cell tumors through molecular cytogenetic studies showing translocation between chromosomes 11 and 22. PNET most commonly presents in adolescents and young adults with pain, swelling, and mass effect. Prognosis depends on tumor site, volume, and presence of metastasis. Treatment involves complete surgical resection when possible along with
1) A 67-year-old male presented with a 4-week history of headaches and memory loss as well as right-sided weakness. MRI showed a brain tumor consistent with a glioblastoma.
2) Glioblastomas are the most common and aggressive primary brain tumors in adults. The standard treatment is maximal surgical resection followed by radiation and chemotherapy with temozolomide, though the median survival is only 12 months.
3) Prognostic factors include age, extent of surgical resection, and performance status. Genetic alterations in pathways such as EGFR and p53 are implicated in glioblastoma pathogenesis. Emerging treatments target these pathways or use immunotherapy, gene therapy, or novel drug
Inter group rhabdomyosarcoma study group (irsg)Ajay Manickam
1. The IRSG study from 1972-1997 evaluated treatment protocols for rhabdomyosarcoma and established a staging and grouping system to determine prognosis and guide therapy.
2. Results showed surgery is important, with Group I having the best outlook while Group IV has the worst. Radiation therapy improved outcomes for Groups II and III. Chemotherapy including VAC or VIE improved failure-free and overall survival.
3. IRSG V recommendations incorporate risk stratification to allow for multidisciplinary treatment tailored to histology, with the goal of local control while preserving function.
This document discusses C-reactive protein (CRP) and its clinical importance. It begins by defining acute phase proteins (APPs) as proteins whose plasma concentration increases or decreases in response to inflammation. CRP is an example of a positive APP whose levels rise with inflammation. It is produced primarily in the liver in response to cytokines like IL-6 and IL-1. Elevated CRP levels can indicate conditions like infections, osteoarthritis, and coronary events. High-sensitivity CRP (hs-CRP) is an even more sensitive marker useful for cardiovascular risk assessment and determining risk of future cardiovascular diseases and events.
This presentation i have made to understand the approach to a kidney biopsy in depth. kidney biopsy is not done in all centers and that's why its difficult to understand it. i have put some cases also to understand it better.
Merkel Cell Carcinoma: From Diagnosis to Treatment (webinar)Natalie Richardson
This document provides an overview of Merkel cell carcinoma, including its histogenesis, pathogenesis, epidemiology, clinical features, diagnosis, staging, treatment options for both localized and metastatic disease, and prognosis. Key points discussed are the role of Merkel cell polyomavirus in pathogenesis, increasing incidence with age and sun exposure, diagnosis through biopsy and immunohistochemistry, standard treatment involving surgery and/or radiation for localized disease and chemotherapy or immunotherapy for advanced stages, and generally poor prognosis especially for metastatic or recurrent disease.
Circumcision early in life protects against carcinoma of the penis by reducing risk of HPV infection and preventing accumulation of smegma. Approximately half of penile carcinomas are HPV-related, with HPV-16 and HPV-18 being the most common types. Symptoms of penile carcinoma include masses, pain, bleeding, groin masses, and urinary symptoms. Diagnosis involves history, physical exam, biopsy, and imaging of lymph nodes. Staging uses the Jackson system or AJCC TNM system, with most cases being well-differentiated squamous cell carcinoma.
A 50-year-old woman presented with abdominal pain, a feeling of masses in her abdomen, and weight loss for three months. Clinical examination revealed two palpable abdominal masses. CT imaging showed multiple masses in the stomach and liver. Differentials included multicentric GIST, adenocarcinoma, and metastasis. Features pointed towards a diagnosis of multicentric GIST with liver metastasis, including the patient's age, well-defined heterogeneous stomach lesions, no lymphadenopathy or calcification, and absence of features against gastric adenocarcinoma.
This document summarizes a case series of 4 patients whose breast cancers were initially misdiagnosed as ductal carcinoma in situ (DCIS) but were later found to be invasive ductal carcinoma based on immunohistochemistry and lymph node involvement. In these cases, the cancers had a morphology that closely mimicked DCIS with central necrosis (comedo-type DCIS) but lacked a myoepithelial cell layer. Immunostains for myoepithelial markers were needed to correctly diagnose the cancers as invasive rather than DCIS and guide appropriate treatment. This case series highlights the importance of confirming DCIS diagnoses with immunohistochemistry to avoid misdiagnosing invasive breast cancers as non-invasive DCIS.
Gastrointestinal stromal tumors (GISTs) are rare mesenchymal tumors that arise from interstitial cells of Cajal in the gastrointestinal tract. GISTs most commonly present in the stomach and small intestine in patients in their late 60s, and median size is 5 cm. While small GISTs are often asymptomatic, larger tumors can cause vague symptoms like abdominal pain or bleeding. Diagnosis involves biopsy or excision of nodules over 2 cm. Immunohistochemistry shows 95% of GISTs are positive for CD117. Prognosis depends on tumor size, mitotic rate, and location. Treatment involves surgery for resectable localized disease and imatinib for advanced or metastatic
A 36-year-old male presented with a single grand mal seizure. MRI showed a well-defined hypodense mass in the left frontal lobe without enhancement or edema. Biopsy revealed a mixed grade II-III diffuse astrocytoma. Diffuse astrocytomas typically present as low-grade tumors that infiltrate the brain without symptoms. They have a tendency to transform into higher grades over time. Radiologically, they appear as well-defined lesions without enhancement or edema. The diagnosis in this case was a mixed grade II-III diffuse astrocytoma based on the MRI and biopsy findings.
Cancer is caused by defects in cell division that result from genetic mutations. Normal cell growth becomes unregulated, as cells multiply uncontrollably and crowd out healthy tissue. If cancer cells invade surrounding areas or spread to other parts of the body through metastasis and angiogenesis, it is considered malignant. Staging and grading of tumors helps determine prognosis and appropriate treatment options like surgery, radiation, chemotherapy, or targeted therapies.
This document contains medical information about a 55-year-old male patient presenting with a 1-year history of an ulcer on his penis, as well as swelling and pain in his groin region and scrotum over the past 8-6 months. Physical examination revealed the penile and groin ulcers, as well as swollen lymph nodes and scrotal enlargement. Biopsy of the penile ulcer showed well-differentiated squamous cell carcinoma. Imaging and tests identified secondary infection with Pseudomonas bacteria and scrotal elephantiasis. The patient was diagnosed with advanced penile cancer complicated by infection and elephantiasis, requiring total penectomy and lymph node dissection for treatment.
Gastrointestinal stromal tumors (GISTs) are rare sarcomas that arise from the gastrointestinal tract. Most commonly found in the stomach, they represent 0.2% of gastrointestinal tumors. While often asymptomatic, they can present with bleeding, pain, or obstruction. Diagnosis involves imaging such as endoscopy or CT scan followed by biopsy showing immunohistochemistry positive for CD117 in 95% of cases. Treatment involves surgical resection with clear margins although adjuvant therapy with imatinib is often used for higher risk tumors. Outcomes have improved greatly in the past two decades with 5-year survival rates now over 50% with appropriate treatment.
1) Ewing's sarcoma is a high-grade malignant bone tumor that most commonly affects children and young adults between 5-30 years old. It arises from bone marrow stem cells and is characterized by small, undifferentiated tumor cells and the translocation mutation t(11;22).
2) Clinically, patients present with pain, swelling, fever, and weight loss near the tumor site. Radiologically, the tumor appears osteolytic and aggressive, often with periosteal reaction. Histologically, it shows small, blue round cells with minimal cytoplasm and rosette formations.
3) Treatment involves chemotherapy, surgery, and radiation therapy. Prognosis is better with localized disease in children and
An MRI scan showed a large heterogeneously enhancing mass lesion in the right frontal region that crossed over to the left frontal region through the corpus callosum, causing mass effect on the lateral ventricles. Features were consistent with glioblastoma multiforme involving both frontal lobes. Glioblastoma multiforme is the most common and most aggressive form of brain cancer, typically occurring in adults between 45-60 years old. Treatment may include surgery, radiation therapy, chemotherapy and experimental therapies, but the cancer often recurs and median survival is less than one year.
This case report describes an 84-year old female patient with a neuroendocrine carcinoma of the breast diagnosed by fine needle aspiration cytology. The smears showed discohesive polygonal cells with abundant cytoplasm and eosinophilic granules. Histology confirmed a solid type neuroendocrine carcinoma with metastasis to lymph nodes. Immunohistochemistry was positive for markers like chromogranin and synaptophysin. Neuroendocrine carcinomas are rare breast tumors that can be diagnosed on cytology by observing characteristic cytoplasmic granules, though they may otherwise appear as invasive ductal carcinoma. Recognition of this rare tumor is important for prognosis and management.
The document discusses carcinoma penis, including its epidemiology, risk factors, pathology, staging, investigations, and treatment options. Premalignant lesions like erythroplasia of Queyrat and balanitis xerotica obliterans are described. Treatment depends on the stage and includes circumcision for small tumors, local excision, glansectomy, Mohs micrographic surgery, and laser surgery to preserve the organ while wide local excision or penectomy may be needed for more advanced cases.
History of DICER1 mutation
DICER1 function
Mutated DICER1 – tumorigenic mechanism
Constellation of lesions associated with DICER1
DICER1 IHC
When to test?
Therapeutic options
The document summarizes updates to the WHO 2020 classification of bone tumors. Key points include:
- Chondroblastoma is now classified as a benign tumor rather than intermediate based on its low metastasis rate.
- 95% of chondroblastomas harbor H3F3A or H3F3B mutations.
- Atypical cartilaginous tumor replaces chondrosarcoma in the appendicular skeleton to reflect variable prognosis between sites.
- Mesenchymal chondrosarcoma is defined by HEY1-NCOA2 fusions in over 90% of cases.
- Osteoblastoma and osteoid osteoma frequently demonstrate FOS/FOSB f
The document discusses recent updates in the diagnosis and grading of prostatic carcinoma, including revisions to Gleason scoring guidelines regarding lesions like cribriform and intraductal carcinoma. It also reviews the role of immunohistochemistry and molecular markers in prognostication as well as emerging applications of artificial intelligence in prostate cancer diagnosis.
Primitive neuroectodermal tumor (PNET) is a highly malignant tumor composed of small round cells of neuroectodermal origin that affects soft tissue and bone. PNETs are classified into groups depending on location, with peripheral PNET (pPNET) occurring in soft tissue and bone outside the central nervous system. pPNET includes Ewing sarcoma and Askin tumor. Diagnosis involves ruling out other small round cell tumors through molecular cytogenetic studies showing translocation between chromosomes 11 and 22. PNET most commonly presents in adolescents and young adults with pain, swelling, and mass effect. Prognosis depends on tumor site, volume, and presence of metastasis. Treatment involves complete surgical resection when possible along with
1) A 67-year-old male presented with a 4-week history of headaches and memory loss as well as right-sided weakness. MRI showed a brain tumor consistent with a glioblastoma.
2) Glioblastomas are the most common and aggressive primary brain tumors in adults. The standard treatment is maximal surgical resection followed by radiation and chemotherapy with temozolomide, though the median survival is only 12 months.
3) Prognostic factors include age, extent of surgical resection, and performance status. Genetic alterations in pathways such as EGFR and p53 are implicated in glioblastoma pathogenesis. Emerging treatments target these pathways or use immunotherapy, gene therapy, or novel drug
Inter group rhabdomyosarcoma study group (irsg)Ajay Manickam
1. The IRSG study from 1972-1997 evaluated treatment protocols for rhabdomyosarcoma and established a staging and grouping system to determine prognosis and guide therapy.
2. Results showed surgery is important, with Group I having the best outlook while Group IV has the worst. Radiation therapy improved outcomes for Groups II and III. Chemotherapy including VAC or VIE improved failure-free and overall survival.
3. IRSG V recommendations incorporate risk stratification to allow for multidisciplinary treatment tailored to histology, with the goal of local control while preserving function.
This document discusses C-reactive protein (CRP) and its clinical importance. It begins by defining acute phase proteins (APPs) as proteins whose plasma concentration increases or decreases in response to inflammation. CRP is an example of a positive APP whose levels rise with inflammation. It is produced primarily in the liver in response to cytokines like IL-6 and IL-1. Elevated CRP levels can indicate conditions like infections, osteoarthritis, and coronary events. High-sensitivity CRP (hs-CRP) is an even more sensitive marker useful for cardiovascular risk assessment and determining risk of future cardiovascular diseases and events.
This presentation i have made to understand the approach to a kidney biopsy in depth. kidney biopsy is not done in all centers and that's why its difficult to understand it. i have put some cases also to understand it better.
This presentation in mainly focused of understanding of automation and its utility in cytopathology. It will be very usefull for postgraduate in pathology, cytopathologist and cytotechnicians.
I have covered all topics related to stem cell and banking of stem cell including collection, storage and thawing of stem cell. I have mentioned some of the stem cell banks available in India too. this is one of the very important question for MD pathology exam. please go through it.
this PPT is all about case base approach to kidney tumors. clinical approach and their radiological findings. indication and contra-indications of Kidney FNAC of Kidney lesions.
This document discusses tuberculosis through a series of case studies. It begins with an introduction to tuberculosis and its morphological features. It then presents 5 case studies involving different organ systems affected by tuberculosis including the lungs, intestines, lymph nodes, bones and brain. Each case provides clinical details, investigation results and gross pathological findings. The document discusses the diagnostic features of tuberculosis in these various organs. It provides images to illustrate primary pulmonary tuberculosis, miliary tuberculosis, intestinal tuberculosis and other forms. The document presents tuberculosis classifications and comparisons to other conditions like cancer.
The document discusses cell blocks, which are used in cytopathology to provide tissue samples from fluid specimens for histological examination. Cell blocks allow for maintaining tissue architecture, performing ancillary tests, and archiving samples. Various cell block preparation methods are described. Cell blocks provide diagnostic advantages over smears for certain tumor types and body fluids. While cell blocks increase diagnostic accuracy, some methods can result in low cellularity or inadequate samples for ancillary testing. Overall, the document provides an overview of the utility and methods of cell block preparation in cytopathology.
The data on thyroid tumors in the fourth edition of the World Health Organization (WHO) classification of endocrine tumors published in 2017 contain significant revisions.
These revisions of the 2004 WHO classification were based on new knowledge about pathology, clinical behavior, and most importantly the genetics of the thyroid tumors.
Autologous Blood Transfusion (ABT) means reinfusion of blood or blood products taken from the same patient
ABT is not a new concept, fear of transfusion- transmitted diseases stimulated the growth of autologous programme
Dr. Manan B. Shah presented on biomarkers for acute kidney injury. The presentation discussed the need for biomarkers to detect AKI earlier than serum creatinine, as creatinine levels typically rise only after 50% kidney function is lost. Several promising urinary biomarkers were described, including NGAL, KIM-1, IL-18, and cystatin C, which can indicate kidney injury earlier. The presentation proposed that a panel of biomarkers may help guide whether renal replacement therapy is needed for patients with AKI. Early detection and treatment of AKI using biomarkers could potentially improve outcomes by preventing or minimizing kidney injury.
Human colors. color of normal and pathologic tissueManan Shah
Colors are important to all living organisms
They are crucial for protection, metabolism, sexual behavior, and communication.
Human organs obviously have color, that is, the liver is brown, the heart is red, bones are white, and so on.
This presentation is focused on diagnostic utility of Red blood cell indices which will be very useful for undergraduate and postgraduate of medical field.
How to Manage Reception Report in Odoo 17Celine George
A business may deal with both sales and purchases occasionally. They buy things from vendors and then sell them to their customers. Such dealings can be confusing at times. Because multiple clients may inquire about the same product at the same time, after purchasing those products, customers must be assigned to them. Odoo has a tool called Reception Report that can be used to complete this assignment. By enabling this, a reception report comes automatically after confirming a receipt, from which we can assign products to orders.
This document provides an overview of wound healing, its functions, stages, mechanisms, factors affecting it, and complications.
A wound is a break in the integrity of the skin or tissues, which may be associated with disruption of the structure and function.
Healing is the body’s response to injury in an attempt to restore normal structure and functions.
Healing can occur in two ways: Regeneration and Repair
There are 4 phases of wound healing: hemostasis, inflammation, proliferation, and remodeling. This document also describes the mechanism of wound healing. Factors that affect healing include infection, uncontrolled diabetes, poor nutrition, age, anemia, the presence of foreign bodies, etc.
Complications of wound healing like infection, hyperpigmentation of scar, contractures, and keloid formation.
Level 3 NCEA - NZ: A Nation In the Making 1872 - 1900 SML.pptHenry Hollis
The History of NZ 1870-1900.
Making of a Nation.
From the NZ Wars to Liberals,
Richard Seddon, George Grey,
Social Laboratory, New Zealand,
Confiscations, Kotahitanga, Kingitanga, Parliament, Suffrage, Repudiation, Economic Change, Agriculture, Gold Mining, Timber, Flax, Sheep, Dairying,
This presentation was provided by Racquel Jemison, Ph.D., Christina MacLaughlin, Ph.D., and Paulomi Majumder. Ph.D., all of the American Chemical Society, for the second session of NISO's 2024 Training Series "DEIA in the Scholarly Landscape." Session Two: 'Expanding Pathways to Publishing Careers,' was held June 13, 2024.
THE SACRIFICE HOW PRO-PALESTINE PROTESTS STUDENTS ARE SACRIFICING TO CHANGE T...indexPub
The recent surge in pro-Palestine student activism has prompted significant responses from universities, ranging from negotiations and divestment commitments to increased transparency about investments in companies supporting the war on Gaza. This activism has led to the cessation of student encampments but also highlighted the substantial sacrifices made by students, including academic disruptions and personal risks. The primary drivers of these protests are poor university administration, lack of transparency, and inadequate communication between officials and students. This study examines the profound emotional, psychological, and professional impacts on students engaged in pro-Palestine protests, focusing on Generation Z's (Gen-Z) activism dynamics. This paper explores the significant sacrifices made by these students and even the professors supporting the pro-Palestine movement, with a focus on recent global movements. Through an in-depth analysis of printed and electronic media, the study examines the impacts of these sacrifices on the academic and personal lives of those involved. The paper highlights examples from various universities, demonstrating student activism's long-term and short-term effects, including disciplinary actions, social backlash, and career implications. The researchers also explore the broader implications of student sacrifices. The findings reveal that these sacrifices are driven by a profound commitment to justice and human rights, and are influenced by the increasing availability of information, peer interactions, and personal convictions. The study also discusses the broader implications of this activism, comparing it to historical precedents and assessing its potential to influence policy and public opinion. The emotional and psychological toll on student activists is significant, but their sense of purpose and community support mitigates some of these challenges. However, the researchers call for acknowledging the broader Impact of these sacrifices on the future global movement of FreePalestine.
A Free 200-Page eBook ~ Brain and Mind Exercise.pptxOH TEIK BIN
(A Free eBook comprising 3 Sets of Presentation of a selection of Puzzles, Brain Teasers and Thinking Problems to exercise both the mind and the Right and Left Brain. To help keep the mind and brain fit and healthy. Good for both the young and old alike.
Answers are given for all the puzzles and problems.)
With Metta,
Bro. Oh Teik Bin 🙏🤓🤔🥰
This presentation was provided by Rebecca Benner, Ph.D., of the American Society of Anesthesiologists, for the second session of NISO's 2024 Training Series "DEIA in the Scholarly Landscape." Session Two: 'Expanding Pathways to Publishing Careers,' was held June 13, 2024.
Philippine Edukasyong Pantahanan at Pangkabuhayan (EPP) CurriculumMJDuyan
(𝐓𝐋𝐄 𝟏𝟎𝟎) (𝐋𝐞𝐬𝐬𝐨𝐧 𝟏)-𝐏𝐫𝐞𝐥𝐢𝐦𝐬
𝐃𝐢𝐬𝐜𝐮𝐬𝐬 𝐭𝐡𝐞 𝐄𝐏𝐏 𝐂𝐮𝐫𝐫𝐢𝐜𝐮𝐥𝐮𝐦 𝐢𝐧 𝐭𝐡𝐞 𝐏𝐡𝐢𝐥𝐢𝐩𝐩𝐢𝐧𝐞𝐬:
- Understand the goals and objectives of the Edukasyong Pantahanan at Pangkabuhayan (EPP) curriculum, recognizing its importance in fostering practical life skills and values among students. Students will also be able to identify the key components and subjects covered, such as agriculture, home economics, industrial arts, and information and communication technology.
𝐄𝐱𝐩𝐥𝐚𝐢𝐧 𝐭𝐡𝐞 𝐍𝐚𝐭𝐮𝐫𝐞 𝐚𝐧𝐝 𝐒𝐜𝐨𝐩𝐞 𝐨𝐟 𝐚𝐧 𝐄𝐧𝐭𝐫𝐞𝐩𝐫𝐞𝐧𝐞𝐮𝐫:
-Define entrepreneurship, distinguishing it from general business activities by emphasizing its focus on innovation, risk-taking, and value creation. Students will describe the characteristics and traits of successful entrepreneurs, including their roles and responsibilities, and discuss the broader economic and social impacts of entrepreneurial activities on both local and global scales.
A Visual Guide to 1 Samuel | A Tale of Two HeartsSteve Thomason
These slides walk through the story of 1 Samuel. Samuel is the last judge of Israel. The people reject God and want a king. Saul is anointed as the first king, but he is not a good king. David, the shepherd boy is anointed and Saul is envious of him. David shows honor while Saul continues to self destruct.
How to Download & Install Module From the Odoo App Store in Odoo 17Celine George
Custom modules offer the flexibility to extend Odoo's capabilities, address unique requirements, and optimize workflows to align seamlessly with your organization's processes. By leveraging custom modules, businesses can unlock greater efficiency, productivity, and innovation, empowering them to stay competitive in today's dynamic market landscape. In this tutorial, we'll guide you step by step on how to easily download and install modules from the Odoo App Store.