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
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
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
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
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
Hepatic bud divides ventral mesogastrium into
-Lesser omentum
Falciform and coronary ligament
Developing spleen divides dorsal mesogastrium into
Gastrosplenic ligament
Lieno renal ligament
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
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
Hamartomas- benign tumorlike nodules composed of overgrowth mature cells and tissues
Arise from splenic embolus or in ass with typhoid and parathyphoid
picture above 1st pic shows splenic abscess dt typhoid infection
Pic shows multiple whitish nodules on cut section
In schistosomiasis, regression of splenomegaly is not possible by medication, hence splenectomy done
Fresh blood transfusion or fresh platelet is required if bleeding is not control by steroid therapy
Hereditary AR
Hypoxia is to be avoided to prevent sickling crisis during general anesthesia
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.
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
Trauma dt accident or during surgical procedure
Removal en bloc – radical gastrectomy, distal or total pancreatectomy
Post splenectomy septicemia
-Strep. Pneumoniae, Neisseria meningitides, Hemophilus influenza, Eschericia coli
-People at risk -Young patient n Patient undergone splenectomy
meningococcus C every 5 years
H. influenzae type every 10 years
Pneumococcal recommended pt 2 years of age