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Lymphadenopathy
Enlarged lymph nodes
Lymph node- basics
 Part of peripheral immune system
 Consist of fibroblasts (trabeculae),
B-cells (germinal center) &
T-cells (paracortical area)
 Function as site for immune cell contact
with antigen, leading to
activation of immune response &
elimination of antigen
LN enlargement- causes
 Increase in immune cells during Ag
response
 Infiltration by inflammatory cells in
infection of LN
 Malignant proliferation of LN cells
 Metastasis
 Infiltration by metabolite laden
macrophages in storage disorders
Evaluation
 Required when LN >1 cm.,
except inguinal >2 cm.
 Factors to consider-
 Age- malignancy more common as age
increases
 Physical charac. of LN- discrete/matted,
firm/hard, mobile/fixed, tender or not
 Node location
 Clinical setting
LNE- site
 Supraclavicular- metastasis from lung/GIT
 L supraclavicular (Virchow’s)- mets from GIT
 B/L epitrochlear- sarcoidosis, tularemia
 U/L axillary- breast cancer, lymphoma, UL
infection, brucellosis, cat-scratch disease
 U/L hilar- lung cancer
 B/L hilar- sarcoidosis, TB, fungal infection,
lymphoma, silicosis, berylliosis
 Inguinal- LL infection, STD (LGV)
Evaluation
 Relevant history- fever, other symptoms
 Examination of LN- size, location,
consistency, mobility, tenderness
 Relevant investigation
 LN FNAC &/or biopsy
Acute & tender LNE- possibly infectious, wait &
watch while treating infection
Splenomegaly
Enlargement of spleen
>12 cm.
Spleen- basics
 A lymphoreticular organ
 Located in LUQ of abdomen
 Normally not palpable
 Structure
 White pulp- B-cell containing follicles &
T-cell in perifollicular/periarteriolar areas
 Red pulp- sinuses & cords lined by
reticuloendothelial cells
Spleen- function
 Clearance of micro-organisms from
blood
 Generation of immune response to
foreign antigens
 Sequestration & removal of blood cells
 Regulation of portal blood flow
 Extramedullary hematopoiesis
Causes of splenomegaly
 Increased function-
 Infection- malaria, kala-azar, IE, TB
 Disordered immunoregulation- Felty’s syndrome
 Increased RBC destruction- spherocytosis, thalassemia,
 Extramedullary hematopoiesis
 Impaired blood flow-
 Cirrhosis
 Thrombosis/obstruction
 Infiltration-
 Amyloidosis, Gaucher/Niemann-Pick disease

Benign/Metastatic SOL
Massive s’megaly- >20 cms.
 CML
 Myelofibrosis
 Kala-azar
 Chronic malaria/TSS
 Thalassemia major
 Portal hypertension
 Sarcoidosis
 Hairy cell leukemia
 Portal vein
obstruction
 Gaucher disease
 Niemann-Pick
disease
Splenomegaly- clinical
Dull dragging LUQ pain
Enlarged spleen
Confirmed by ultrasound
Hypersplenism
 Splenomegaly
 Cytopenia
 Hypercellular bone-marrow
 Peripheral evidence of increased
production of cell line affected
 Immediate response after splenectomy
Treatment
Of underlying disease.
Splenectomy, if required
(trauma, hypersplenism)
Hepatomegaly
Liver has many functions
Hepatomegaly- causes
 Infection- IM, hepatitis, malaria
 Granulomatous- TB, sarcoidosis
 Neoplasm- secondaries, HCC, lymphoma,
hemangioma
 Congestion- CHF, hepatic vein thrombosis
 Infiltration- NASH, hemochromatosis,
amyloidosis, Gaucher/Niemann-Pick disease
 Other- ALA, hydatid cyst, ADPKD
Hepatomegaly- clinical
 h/o jaundice, RUQ pain
 Examination- liver span by percussion
 Liver- tender, soft/hard, smooth or not
 LFT-
 Structural- SGPT, alkaline phosphatase, GGT
 Functional- albumin, INR
 Ultrasound
 CT scan
Treatment
Underlying cause

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Lymphadenopathy & splenomegaly & hepatomegaly

  • 2. Lymph node- basics  Part of peripheral immune system  Consist of fibroblasts (trabeculae), B-cells (germinal center) & T-cells (paracortical area)  Function as site for immune cell contact with antigen, leading to activation of immune response & elimination of antigen
  • 3. LN enlargement- causes  Increase in immune cells during Ag response  Infiltration by inflammatory cells in infection of LN  Malignant proliferation of LN cells  Metastasis  Infiltration by metabolite laden macrophages in storage disorders
  • 4. Evaluation  Required when LN >1 cm., except inguinal >2 cm.  Factors to consider-  Age- malignancy more common as age increases  Physical charac. of LN- discrete/matted, firm/hard, mobile/fixed, tender or not  Node location  Clinical setting
  • 5. LNE- site  Supraclavicular- metastasis from lung/GIT  L supraclavicular (Virchow’s)- mets from GIT  B/L epitrochlear- sarcoidosis, tularemia  U/L axillary- breast cancer, lymphoma, UL infection, brucellosis, cat-scratch disease  U/L hilar- lung cancer  B/L hilar- sarcoidosis, TB, fungal infection, lymphoma, silicosis, berylliosis  Inguinal- LL infection, STD (LGV)
  • 6. Evaluation  Relevant history- fever, other symptoms  Examination of LN- size, location, consistency, mobility, tenderness  Relevant investigation  LN FNAC &/or biopsy Acute & tender LNE- possibly infectious, wait & watch while treating infection
  • 8. Spleen- basics  A lymphoreticular organ  Located in LUQ of abdomen  Normally not palpable  Structure  White pulp- B-cell containing follicles & T-cell in perifollicular/periarteriolar areas  Red pulp- sinuses & cords lined by reticuloendothelial cells
  • 9. Spleen- function  Clearance of micro-organisms from blood  Generation of immune response to foreign antigens  Sequestration & removal of blood cells  Regulation of portal blood flow  Extramedullary hematopoiesis
  • 10. Causes of splenomegaly  Increased function-  Infection- malaria, kala-azar, IE, TB  Disordered immunoregulation- Felty’s syndrome  Increased RBC destruction- spherocytosis, thalassemia,  Extramedullary hematopoiesis  Impaired blood flow-  Cirrhosis  Thrombosis/obstruction  Infiltration-  Amyloidosis, Gaucher/Niemann-Pick disease  Benign/Metastatic SOL
  • 11. Massive s’megaly- >20 cms.  CML  Myelofibrosis  Kala-azar  Chronic malaria/TSS  Thalassemia major  Portal hypertension  Sarcoidosis  Hairy cell leukemia  Portal vein obstruction  Gaucher disease  Niemann-Pick disease
  • 12. Splenomegaly- clinical Dull dragging LUQ pain Enlarged spleen Confirmed by ultrasound
  • 13. Hypersplenism  Splenomegaly  Cytopenia  Hypercellular bone-marrow  Peripheral evidence of increased production of cell line affected  Immediate response after splenectomy
  • 14. Treatment Of underlying disease. Splenectomy, if required (trauma, hypersplenism)
  • 16. Hepatomegaly- causes  Infection- IM, hepatitis, malaria  Granulomatous- TB, sarcoidosis  Neoplasm- secondaries, HCC, lymphoma, hemangioma  Congestion- CHF, hepatic vein thrombosis  Infiltration- NASH, hemochromatosis, amyloidosis, Gaucher/Niemann-Pick disease  Other- ALA, hydatid cyst, ADPKD
  • 17. Hepatomegaly- clinical  h/o jaundice, RUQ pain  Examination- liver span by percussion  Liver- tender, soft/hard, smooth or not  LFT-  Structural- SGPT, alkaline phosphatase, GGT  Functional- albumin, INR  Ultrasound  CT scan