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NUR FADZLINA ZABRI
082013100006
Embryology
 Condensations of mesogastrium in dorsal
mesogastrium
Anatomy
Functions of spleen
• Immune function – major site of IgM
production and opsonins
• Filter function – cellular and non cellular
• Reservoir function – contains 8% of red cell
mass
• Hematopoesis – in fetal life and hematological
disorder
Investigations
• History – pain, infection, hemolytic disease in
family
• Examination findings – splenomegaly, splenic
bruit
• Laboratory examination – full blood count,
reticulocyte count, hemolytic test
• Radiological imaging – plain radiology, US,CT,
MRI
DISEASES OF SPLEEN
A) Spleen anomalies
i. Splenic agenesis
ii. Polysplenia – results from failure of splenic fusion
iii. Splenunculi – single/multiple spleen accessory
iv. Hamartomas
v. Non parasitic splenic cyst
B) Splenic artery aneurysm, infarct and rupture
Splenic artery rupture
• Associated with atherosclerotic patient
• Consequence of intraabdominal sepsis or
pancreatic necrosis
• Presence of splenic bruit
•Detected on Xray or scan
•Treatment – splenectomy and removal of diseased
artery
Splenic infarction
Massive splenomegaly :
• Myeloproliferative
syndrome
• Portal hypertension
• Splenic vein
thrombosis
• Sickle cell disease
- Left shoulder tip
pain
- Infarct causing
abscess requires
splenectomy
Splenic rupture
Causes ;
- Blunt abdominal
trauma
- Iatrogenic injury
Rupture of malarial
spleen
- Rupture of enlarged
spleen due to
malaria
- Must undergo
splenectomy before
perisplenic
hematoma ruptures
C) Splenomegaly and hypersplenism
Splenic abscess
– Rare- should be suspected
when there is progressive
splenic enlargement with
bacteremia and abscess
formation at other sites
– Associated with
– Pancreatic necrosis
– Intra abdominal infection
– Care : percutaneus drainage
of the splenic abscess under
radiological guidance
Tuberculosis of spleen
– Young adults with splenomegaly : asthenia, loss of weight,
fever
– Anti tuberculous drug
– Splenectomy is difficult
Tropical splenomegaly
– Occurs in tropical country
– Malaria
– Kalazar
– Schistosomiasis
– Occult infection
– Malnutrition
– Requires splenectomy
Results from portal
hypertension associated with
Hepatic fibrosis
or
Hyperplasia of induced
phagocytosis of disintegrated
worms, ova or toxin
Idiopathic thrombocytopenic purpura
– Antibodies develop against platelet membrane
glycoprotein that damages patient’s platelet
– Features
– Purpuric patches on skin and mucosa
(ecchymoses)
– Numbers of petechial hemorrhages
– Tendency of spontaneous bleeding
– Corticosteroids
– Steroid relapses or platelet remains low 
splenectomy
Hemolytic anemia
Hereditary spherocytosis
• AD hereditary disorder
• Presence of spherocytic red cells, various in
molecular defects in the gene
• Mild jaundice, anemia, splenomegaly and
gallstones
• Splenectomy done after 6 years of age
Thalassemia
• Defects in the hemoglobin
peptide chain synthesis
• Chronic anemia, jaundice,
splenomegaly, hemolytic
facies
• Requires blood transfusion
• Splenectomy ;
• Transfusion dependent
• Hemolytic antibodies develop
Sickle cell anemia
• Hb A is being replaced by Hb S
• Hb S crystallises when oxygen tension is
reduce  distorting elongated red cell
• Increase blood viscosity
• Obstruct the flow of blood in spleen
Crisis – adequate hydration, partial exchange transfusion
Splenectomy in splenic sequestration aggravates anemia
Porphyria
– Hereditary error of hemoglobin catabolism
– Features :
• Abdominal crises – intestinal colic, constipation
• Anemic
• Photosensitivity
• Splenomegaly
• Port-wine colour urine
– Splenectomy has little role in management
Gauchers disease
– Defect of glycosphingolipid metabolism- accumulation
of glucocerebroside
– Enormous splenic enlargement + yellowish brown
discoloration of skin, anemia, conjunctival thickening
Hypersplenism due to portal hypertension
– Results in thrombytopenia and granulocytopenia
– Care : shunt surgery or liver transplantation
– Symptomatic esophagogastric varices requires
splenectomy
Felty’s syndrome
Treated with steroids or splenectomy
• Common benign tumor of spleen
• Rarely develop into hemangiosarcoma
• Treatment – splenectomy
D) Neoplasm
Hemangioma
Lymphoma
• Common cause of neoplastic enlargement
• Splenectomy is required for achieving the
diagnosis in the absence of palpable lymph
node or
• Relieving gross splenomegaly
• Results from abnormal proliferation of
mesenchymal elements in the bone marrow,
spleen, liver, lymph node
• Pain due to gross enlargement or splenic
infarction
• Splenectomy
Myelofibrosis
INDICATIONS
• Trauma
• Oncological – part en bloc resection,
therapeutic, diagnostic
• To reduce anemia or thrombocytopenia in
spherocytosis, ITP, hypersplenism
• Variceal surgery for portal hypertension
SPLENECTOMY
Preoperative preparation
Coagulation profile
– Should be near normal
– Bleeding tendency – blood transfucion, FFP,
cryoprecipitate, platelets
Antibiotic prophylaxis
– To prevent post-splenectomy sepsis
Technique of open splenectomy
Midline or transverse left subcostal
incision or thoracoabdominal incision
Gastrosplenic ligament is open up,
short gastric vessels are divided
Splenic vessels are suture-ligated
Posterior surface of spleen is ligated
Lienorenal ligament is divided with
long curved scissors
Spleen is rotated medially along with
the tail and body of the pancreas
Pancreas is separated from the hilar
vessels, ligated and divided
Hemostasis
• Ligation or application of metal clips to
intrasplenic vessels
• Application of hemostatic agents or mesh
A long incision is
made from the
xiphoid process
down to just
below umbilicus
Splenic blood
vessels are
ligated and the
spleen is
dissected out
The vessels are
tied off and the
packing is
removed
Packing is
placed in the
abdomen to
stop the
bleeding.
Blunt
dissection is
then used to
locate the
source od
hemorrhage
Technique of laparoscopic splenectomy
Spleen is separated from the
kidney and diaphragm
Pulled the liver aside
Pull back the stomach to reveal
the spleen
Spleen tissue are then cut.
Self retaining opening bag
is introduced and spleen is
broken into smaller pieces
Splenic artery and vein are
closed off and cut
• Hemorrhage dt slipped ligature
• Hematemesis dt gastric mucosal damage
• Left basal atelectasis, Pleural effusion
• Fistula from damage of the greater curvature of
stomach
• Pancreatitis , localised abscess
• Postoperative thrombocytosis
• Post splenectomy septicemia
• Opportunist post-splenectomy infection
Post operative complication
Opportunist post-splenectomy infection
(OPSI)
Recommendations
– Immunisation
– Antibiotic prophylaxis
– Education : travel advise
– Prompt treatment of infection
Antibiotic prophylaxis
– Oral penicillin,erythromycin, amoxicillin, co-
amoxiclav
– <5 years age : daily dose of penicillin for 10 years
– Older children : prophylaxis is continued till 16
years of age
Immunization
– Vaccination against pneumococcus,
meningococcus C, H. influenzae type B
– Given 2 weeks before elective surgery or as soon
as possible as recovery from surgery
Allergy to penicillin– cefotaxime,
ceftriaxone, chloramphenicol
Education
– Should carry medical alert and Up to date
vaccination card
– Give specific advice on
– travel : use all physical anti-mosquito
barriers, anti-malarial therapy
– animal handling : Capnocytophaga
canimorsus
REFERENCES
• Bailey and Love
• https://www.youtube.com/watch?v=gC0aaE7J
W2Y
• http://preop.com/

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Diseases of Spleen

  • 2. Embryology  Condensations of mesogastrium in dorsal mesogastrium
  • 3.
  • 5.
  • 6. Functions of spleen • Immune function – major site of IgM production and opsonins • Filter function – cellular and non cellular • Reservoir function – contains 8% of red cell mass • Hematopoesis – in fetal life and hematological disorder
  • 7. Investigations • History – pain, infection, hemolytic disease in family • Examination findings – splenomegaly, splenic bruit • Laboratory examination – full blood count, reticulocyte count, hemolytic test • Radiological imaging – plain radiology, US,CT, MRI
  • 8. DISEASES OF SPLEEN A) Spleen anomalies i. Splenic agenesis ii. Polysplenia – results from failure of splenic fusion iii. Splenunculi – single/multiple spleen accessory iv. Hamartomas v. Non parasitic splenic cyst
  • 9. B) Splenic artery aneurysm, infarct and rupture Splenic artery rupture • Associated with atherosclerotic patient • Consequence of intraabdominal sepsis or pancreatic necrosis • Presence of splenic bruit •Detected on Xray or scan •Treatment – splenectomy and removal of diseased artery
  • 10. Splenic infarction Massive splenomegaly : • Myeloproliferative syndrome • Portal hypertension • Splenic vein thrombosis • Sickle cell disease - Left shoulder tip pain - Infarct causing abscess requires splenectomy
  • 11. Splenic rupture Causes ; - Blunt abdominal trauma - Iatrogenic injury Rupture of malarial spleen - Rupture of enlarged spleen due to malaria - Must undergo splenectomy before perisplenic hematoma ruptures
  • 12. C) Splenomegaly and hypersplenism
  • 13.
  • 14. Splenic abscess – Rare- should be suspected when there is progressive splenic enlargement with bacteremia and abscess formation at other sites – Associated with – Pancreatic necrosis – Intra abdominal infection – Care : percutaneus drainage of the splenic abscess under radiological guidance
  • 15. Tuberculosis of spleen – Young adults with splenomegaly : asthenia, loss of weight, fever – Anti tuberculous drug – Splenectomy is difficult
  • 16. Tropical splenomegaly – Occurs in tropical country – Malaria – Kalazar – Schistosomiasis – Occult infection – Malnutrition – Requires splenectomy Results from portal hypertension associated with Hepatic fibrosis or Hyperplasia of induced phagocytosis of disintegrated worms, ova or toxin
  • 17. Idiopathic thrombocytopenic purpura – Antibodies develop against platelet membrane glycoprotein that damages patient’s platelet – Features – Purpuric patches on skin and mucosa (ecchymoses) – Numbers of petechial hemorrhages – Tendency of spontaneous bleeding – Corticosteroids – Steroid relapses or platelet remains low  splenectomy
  • 18. Hemolytic anemia Hereditary spherocytosis • AD hereditary disorder • Presence of spherocytic red cells, various in molecular defects in the gene • Mild jaundice, anemia, splenomegaly and gallstones • Splenectomy done after 6 years of age
  • 19. Thalassemia • Defects in the hemoglobin peptide chain synthesis • Chronic anemia, jaundice, splenomegaly, hemolytic facies • Requires blood transfusion • Splenectomy ; • Transfusion dependent • Hemolytic antibodies develop
  • 20. Sickle cell anemia • Hb A is being replaced by Hb S • Hb S crystallises when oxygen tension is reduce  distorting elongated red cell • Increase blood viscosity • Obstruct the flow of blood in spleen Crisis – adequate hydration, partial exchange transfusion Splenectomy in splenic sequestration aggravates anemia
  • 21. Porphyria – Hereditary error of hemoglobin catabolism – Features : • Abdominal crises – intestinal colic, constipation • Anemic • Photosensitivity • Splenomegaly • Port-wine colour urine – Splenectomy has little role in management
  • 22. Gauchers disease – Defect of glycosphingolipid metabolism- accumulation of glucocerebroside – Enormous splenic enlargement + yellowish brown discoloration of skin, anemia, conjunctival thickening
  • 23. Hypersplenism due to portal hypertension – Results in thrombytopenia and granulocytopenia – Care : shunt surgery or liver transplantation – Symptomatic esophagogastric varices requires splenectomy
  • 24. Felty’s syndrome Treated with steroids or splenectomy
  • 25. • Common benign tumor of spleen • Rarely develop into hemangiosarcoma • Treatment – splenectomy D) Neoplasm Hemangioma
  • 26. Lymphoma • Common cause of neoplastic enlargement • Splenectomy is required for achieving the diagnosis in the absence of palpable lymph node or • Relieving gross splenomegaly
  • 27. • Results from abnormal proliferation of mesenchymal elements in the bone marrow, spleen, liver, lymph node • Pain due to gross enlargement or splenic infarction • Splenectomy Myelofibrosis
  • 28. INDICATIONS • Trauma • Oncological – part en bloc resection, therapeutic, diagnostic • To reduce anemia or thrombocytopenia in spherocytosis, ITP, hypersplenism • Variceal surgery for portal hypertension SPLENECTOMY
  • 29. Preoperative preparation Coagulation profile – Should be near normal – Bleeding tendency – blood transfucion, FFP, cryoprecipitate, platelets Antibiotic prophylaxis – To prevent post-splenectomy sepsis
  • 30. Technique of open splenectomy Midline or transverse left subcostal incision or thoracoabdominal incision Gastrosplenic ligament is open up, short gastric vessels are divided Splenic vessels are suture-ligated
  • 31. Posterior surface of spleen is ligated Lienorenal ligament is divided with long curved scissors Spleen is rotated medially along with the tail and body of the pancreas Pancreas is separated from the hilar vessels, ligated and divided
  • 32. Hemostasis • Ligation or application of metal clips to intrasplenic vessels • Application of hemostatic agents or mesh
  • 33. A long incision is made from the xiphoid process down to just below umbilicus Splenic blood vessels are ligated and the spleen is dissected out The vessels are tied off and the packing is removed Packing is placed in the abdomen to stop the bleeding. Blunt dissection is then used to locate the source od hemorrhage
  • 35. Spleen is separated from the kidney and diaphragm Pulled the liver aside Pull back the stomach to reveal the spleen Spleen tissue are then cut.
  • 36. Self retaining opening bag is introduced and spleen is broken into smaller pieces Splenic artery and vein are closed off and cut
  • 37.
  • 38. • Hemorrhage dt slipped ligature • Hematemesis dt gastric mucosal damage • Left basal atelectasis, Pleural effusion • Fistula from damage of the greater curvature of stomach • Pancreatitis , localised abscess • Postoperative thrombocytosis • Post splenectomy septicemia • Opportunist post-splenectomy infection Post operative complication
  • 39. Opportunist post-splenectomy infection (OPSI) Recommendations – Immunisation – Antibiotic prophylaxis – Education : travel advise – Prompt treatment of infection
  • 40. Antibiotic prophylaxis – Oral penicillin,erythromycin, amoxicillin, co- amoxiclav – <5 years age : daily dose of penicillin for 10 years – Older children : prophylaxis is continued till 16 years of age Immunization – Vaccination against pneumococcus, meningococcus C, H. influenzae type B – Given 2 weeks before elective surgery or as soon as possible as recovery from surgery Allergy to penicillin– cefotaxime, ceftriaxone, chloramphenicol
  • 41. Education – Should carry medical alert and Up to date vaccination card – Give specific advice on – travel : use all physical anti-mosquito barriers, anti-malarial therapy – animal handling : Capnocytophaga canimorsus
  • 42. REFERENCES • Bailey and Love • https://www.youtube.com/watch?v=gC0aaE7J W2Y • http://preop.com/

Editor's Notes

  1. Hepatic bud divides ventral mesogastrium into -Lesser omentum Falciform and coronary ligament Developing spleen divides dorsal mesogastrium into Gastrosplenic ligament Lieno renal ligament
  2. 75-250g -Lies in left hypochondrium, between fundus of stomach and left hemidiaphragm, long axis lies along 10th ribs - Hilum sits in the angle between stomach and kidney, and in contact with tail of the pancreas
  3. Igm – phagocytic, bactericidal, and tumoricidal activity Cellular – old platelet and rbcs, iron from degraded Hb to return back to serum Non celullar – bacterial infection mainly pneumococci
  4. Hamartomas- benign tumorlike nodules composed of overgrowth mature cells and tissues
  5. Arise from splenic embolus or in ass with typhoid and parathyphoid picture above 1st pic shows splenic abscess dt typhoid infection
  6. Pic shows multiple whitish nodules on cut section
  7. In schistosomiasis, regression of splenomegaly is not possible by medication, hence splenectomy done
  8. Fresh blood transfusion or fresh platelet is required if bleeding is not control by steroid therapy
  9. Hereditary AR
  10. Hypoxia is to be avoided to prevent sickling crisis during general anesthesia
  11.  abnormal metabolism of the blood pigment haemoglobin. Porphyrins are excreted in the urine, which becomes dark; other symptoms include mental disturbances and extreme sensitivity of the skin to light.
  12. serious bone marrow disorder that disrupts your body's normal production of blood cells. The result is extensive scarring in your bone marrow, leading to severe anemia, weakness, fatigue, and often, an enlarged spleen and liver
  13. Trauma dt accident or during surgical procedure Removal en bloc – radical gastrectomy, distal or total pancreatectomy
  14. Post splenectomy septicemia -Strep. Pneumoniae, Neisseria meningitides, Hemophilus influenza, Eschericia coli -People at risk -Young patient n Patient undergone splenectomy
  15. meningococcus C every 5 years H. influenzae type every 10 years Pneumococcal recommended pt 2 years of age