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SPLENOMEGALY :
APPROACH
By-
FAHADAHMAD
RN-27
FINALYEARMBBSHIMSR
INTRODUCTION
Anatomy & Physiology
Classification
Etiology
Step-wise approach
Associated features
Investigations
ANATOMY
• develops from condensations of mesoderm in the dorsal
mesogastrium.
• The weight of the normal adult spleen is 75–250 g.
• lies in the left hypochondrium between the gastric
fundus and the left hemidiaphragm, with its long axis
lying along the tenth rib.
• The hilum sits in the angle between the stomach and the
kidney and is in contact with the tail of the pancreas.
The lower pole extends no further than the mid-axillaryline.
There is a notch on the inferolateral border, and this may be palpated
when the spleen is enlarged.
Normal spleen
Normal size
12 cm length , 7 cm width
13cm craniocaudal diameter
Weight < 250gm
Located along- 9th, 10th,11th ribs mid-axillary
Spleen should be twice the size to be PALPABLE
Palpable spleens are not always ABNORMAL
3% normal population has palpable spleen
Splenomegaly : Spleen weight of 400-500gm
750 – 1000gm : prominent below costal margin
>1000gm : massive splenomegaly
EXAMINATION OF SPLEEN
INSPECTION :Fullness in LUQ that descends on inspiration
Situated behind 9th, 10th and 11th ribs
Long axis along line of 10th rib
Anteriorly extends upto mid axillaryline
Posteriorly, the superior angle is 4cm lateral to D10spine
PALPATION
BIMANUALPALPATION
BALLOTMENT
PALPATION FROMABOVE- MIDDLETON MANOUVRE
BIMANUAL PALPATION
1. Place left palm firmly over left costal margin posterolaterally and
press it forward and medially.
Palpate spleen with right hand starting from right iliacfossa
BIMANUAL PALPATION
2. Turn patient to right lateralposition
Palpate with right hand
MIDDLETON MANOUVRE
Stand on left side
Face foot end of patient
Hooked fingers of LEFTHAND placed
under left costal margin
With right hand, pressure isexerted
over posterolateral aspect of lower
thorax
PERCUSSION
NIXONSMETHOD
Right lateral decubitus
Start from posterior axillaryline
Upper border of dullness normally 6-8cm above costalmargin
>8cm dullness  splenic enlargement
PERCUSSION
CASTELLSMETHOD
Supine position
Dull note over lowest ICSin Anterior axillary line on full inspiration
indicate splenomegaly
PERCUSSION
TRAUBE’SSEMILUNAR SPACE
left sixth rib superiorly
left anterior axillary linelaterally
left costal margin inferiorly
Dull note :splenomegaly
Differential diagnosis
Enlarged left kidney
Enlarged left lobe liver
Carcinoma stomach
Carcinoma splenic flexure colon
Omental mass
Malignancy tail of pancreas
splenomegaly
Massive
Moderate
Mild
beyond umblicus, crosses mid line
>8cm below left costal margin and or >1000gm weight
b/w costal margin & umblicus
(4-8cm)
just palpable
(1-3cm)
MECHANISM of SPLENOMEGALY
1. Hyperplasia or hypertrophy
Reticuloendothelial hyperplasia
Immune hyperplasia in response to
A. systemic infection
B. immunological diseases
2. Passive congestion due to decreased blood flow
3. Infiltrative diseases
CAUSESOFSPLENOMEGALY
Inflammatory splenomegaly
Hyperplastic splenomegaly
Infectious splenomegaly
Congestive splenomegaly
Infiltrative splenomegaly
INCREASEDDEMAND FOR
SPLENIC FUNCTION
1. INCREASED DEMAND
A. RETICULOENDOTHELIALSYSTEMHYPERPLASIA
Spherocytosis
Early sickle cellanemia
Ovalocytosis
Thalassemia major
Hemoglobinopathies
PNH
Pernicious anemia
INCREASED DEMAND
B.IMMUNE HYPERPLASIA
Hi
(i) Response to infection IMN, viral hepatitis,AIDS,CMV,IE,TB,
stoplasmosis, Malaria,Bacterial sepsis,Cong syphilis, splenic abscess,
Leishmaniasis, Trypanosmiasis, Ehrlichiosis
(ii) Disordered Immunoregulation RA(Felty syndrome), SLE,Collagen
vascular diseases,AIHA,Immune thrombocytopenias, Drug reactions,
Sarcoidosis, Interleukin2 therapy,Thyrotoxicosis
(iii) Extramedullary hematopoiesis : Myelofibrosis, Myeloinfiltrative
disorders, marrow damage by toxins,radiation.
2. Abnormal splenic/portal blood flow
Cirrhosis
Hepatic vein obstruction
Portal vein obstruction
Cavernous transformation of portal vein
Splenic vein obstruction
Splenic artery aneurysm
Hepatic schistosomiasis
CHF
Hepatic echinococcosis
Portal hypertension
3. Infiltration of Spleen
 deposits
 Amyloidosis
 Gaucher disease
 Niemann Pick
 Tangier disease
 Hurlers syndrome, Other
MPS
 Hyperlipidemias
Intracellular or extracellular
Leukemias
Benign and Malignant Infiltrations
Lymphomas
Hodgkins disease
Myeloproliferative syndromes
Angiosarcomas
Metastasis ( MC= Melanoma)
Eosinophilic Granuloma
Histiocytosis X
Hamartomas
Hemangioma
Splenic cysts
4. Unknown Etiology
Idiopathic splenomegaly
Berylliosis
Iron deficiencyanemia
MASSIVE SPLENOMEGALY
(>1000GM or >8cm)
CML
CLL
Lymphoma
Hairy cell leukemia
Myelofibrosis with myeloid metaplasia
Chronic malaria
Kala - azar (Tropical Splenomegaly)
Sarcoidosis
Gaucher disease
AIHA
Diffuse splenic hemangiomatosis
Moderate splenomegaly(4-8cm)
Viral hepatitis
Cirrhosis
Lymphomas
Amyloidosis
Splenic abscess,infarct
Hemolytic anemias
IMN
Hemochromatosis
Polycythemias
Mild splenomegaly (1-3cm)
Acute malaria
Typhoid
kala-azar
Septicemias
SLE
Infective endocarditis
RA
Thalassemia Minor
Miliary TB
Leptospirosis
HIV
CCF
Step-wise approach to splenomegaly
History
Physical examination
Laboratory tests
Imaging
Specialised tests
History
Mild vague, abdominal pain.
Pain may be referred to the left shoulder.
Early satiety from gastric displacement occurs with massive splenomegaly.
Associated symptoms or signs
Febrile illness (infectious)
Pallor, dyspnea, bruising, and/or petechiae (hemolytic process)
History of liver disease (congestive)
Weight loss, constitutional symptoms (neoplastic)
Pancreatitis (splenic vein thrombosis)
Alcoholism, hepatitis (cirrhosis)
Special situations associated with
splenomegaly
Fever -typhoid,malaria,kalaazar, infect.endocarditis,
leukemia,lymphoma
Tender spleen - rupture,abscess,infarct
a/c illness + anemia- AIHA,leukemia
Fever + LN- IMN, leukemia, lymhomas, SLE, sarcoid
Anemia- hemolytic anemia, hemoglobinopathies
Jaundice – cirrhosis, hemolytic anemia
Pulsatile spleen- aneurysm
High ESR-connective tissuedisorder
Leukopenia- felty’s syndrome, septicemia
Physical examination
Size of the spleen
Hepatomegaly
Lymphadenopathy
Fever
Icterus
Bruising,petechiae
Oral & supf.sepsis
Stigmata of liver disease
Stigmata of RA/SLE
Splinter hemorrhage,retinal hemorrhage
Cardiac murmurs
Lab investigations
CBC
Peripheral smear study
Reticulocyte count
Blood C/S
Serology (viral, parasitic)
LFT
Hb electrophoresis / coombs test
Coagulation profile
Amylase/lipase
AMA, Anti CCP
,RAfactor
Bone marrow analysis
Imaging
USG
CTscan
sensitive & specificnon-invasive
- etiology of splenomegaly
- liver size,heterogenecity
- splenic mets, abscess,calcf.,cysts
- retro peritoneal LN
- cranio caudal ln > 12cm
Liver- spleen colloid scan- (RBC–Cr51,Tc99)
- hepatic steatosis, SOL,splenic functions
- PHT,colloid shift +
MRI/ Doppler USG - portal / splenic veinthrombosis
- cavernomas
imaging
MRI scanliver hemangiomas
hemochromatosis
erlenmeyer flask sign (Gaucher)
PETscan Dx & staging of lymphomas
determine metabolic cells in spleen
Specialised testing
Abdominal fat pad aspiration
JAK-2 mutation
Gene testing (bcr-abl ,C282Y)
Enzyme testing
Lymph node biopsy
FNAC spleen
Splenectomy
Liver biopsy
Spleenomegaly.pptx

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Spleenomegaly.pptx

  • 2. INTRODUCTION Anatomy & Physiology Classification Etiology Step-wise approach Associated features Investigations
  • 3. ANATOMY • develops from condensations of mesoderm in the dorsal mesogastrium. • The weight of the normal adult spleen is 75–250 g. • lies in the left hypochondrium between the gastric fundus and the left hemidiaphragm, with its long axis lying along the tenth rib. • The hilum sits in the angle between the stomach and the kidney and is in contact with the tail of the pancreas.
  • 4. The lower pole extends no further than the mid-axillaryline. There is a notch on the inferolateral border, and this may be palpated when the spleen is enlarged.
  • 5. Normal spleen Normal size 12 cm length , 7 cm width 13cm craniocaudal diameter Weight < 250gm Located along- 9th, 10th,11th ribs mid-axillary Spleen should be twice the size to be PALPABLE Palpable spleens are not always ABNORMAL 3% normal population has palpable spleen
  • 6. Splenomegaly : Spleen weight of 400-500gm 750 – 1000gm : prominent below costal margin >1000gm : massive splenomegaly
  • 7.
  • 8. EXAMINATION OF SPLEEN INSPECTION :Fullness in LUQ that descends on inspiration Situated behind 9th, 10th and 11th ribs Long axis along line of 10th rib Anteriorly extends upto mid axillaryline Posteriorly, the superior angle is 4cm lateral to D10spine
  • 10. BIMANUAL PALPATION 1. Place left palm firmly over left costal margin posterolaterally and press it forward and medially. Palpate spleen with right hand starting from right iliacfossa
  • 11. BIMANUAL PALPATION 2. Turn patient to right lateralposition Palpate with right hand
  • 12. MIDDLETON MANOUVRE Stand on left side Face foot end of patient Hooked fingers of LEFTHAND placed under left costal margin With right hand, pressure isexerted over posterolateral aspect of lower thorax
  • 13. PERCUSSION NIXONSMETHOD Right lateral decubitus Start from posterior axillaryline Upper border of dullness normally 6-8cm above costalmargin >8cm dullness  splenic enlargement
  • 14. PERCUSSION CASTELLSMETHOD Supine position Dull note over lowest ICSin Anterior axillary line on full inspiration indicate splenomegaly
  • 15. PERCUSSION TRAUBE’SSEMILUNAR SPACE left sixth rib superiorly left anterior axillary linelaterally left costal margin inferiorly Dull note :splenomegaly
  • 16. Differential diagnosis Enlarged left kidney Enlarged left lobe liver Carcinoma stomach Carcinoma splenic flexure colon Omental mass Malignancy tail of pancreas
  • 17. splenomegaly Massive Moderate Mild beyond umblicus, crosses mid line >8cm below left costal margin and or >1000gm weight b/w costal margin & umblicus (4-8cm) just palpable (1-3cm)
  • 18. MECHANISM of SPLENOMEGALY 1. Hyperplasia or hypertrophy Reticuloendothelial hyperplasia Immune hyperplasia in response to A. systemic infection B. immunological diseases 2. Passive congestion due to decreased blood flow 3. Infiltrative diseases
  • 19. CAUSESOFSPLENOMEGALY Inflammatory splenomegaly Hyperplastic splenomegaly Infectious splenomegaly Congestive splenomegaly Infiltrative splenomegaly INCREASEDDEMAND FOR SPLENIC FUNCTION
  • 20. 1. INCREASED DEMAND A. RETICULOENDOTHELIALSYSTEMHYPERPLASIA Spherocytosis Early sickle cellanemia Ovalocytosis Thalassemia major Hemoglobinopathies PNH Pernicious anemia
  • 21. INCREASED DEMAND B.IMMUNE HYPERPLASIA Hi (i) Response to infection IMN, viral hepatitis,AIDS,CMV,IE,TB, stoplasmosis, Malaria,Bacterial sepsis,Cong syphilis, splenic abscess, Leishmaniasis, Trypanosmiasis, Ehrlichiosis (ii) Disordered Immunoregulation RA(Felty syndrome), SLE,Collagen vascular diseases,AIHA,Immune thrombocytopenias, Drug reactions, Sarcoidosis, Interleukin2 therapy,Thyrotoxicosis (iii) Extramedullary hematopoiesis : Myelofibrosis, Myeloinfiltrative disorders, marrow damage by toxins,radiation.
  • 22. 2. Abnormal splenic/portal blood flow Cirrhosis Hepatic vein obstruction Portal vein obstruction Cavernous transformation of portal vein Splenic vein obstruction Splenic artery aneurysm Hepatic schistosomiasis CHF Hepatic echinococcosis Portal hypertension
  • 23. 3. Infiltration of Spleen  deposits  Amyloidosis  Gaucher disease  Niemann Pick  Tangier disease  Hurlers syndrome, Other MPS  Hyperlipidemias Intracellular or extracellular Leukemias Benign and Malignant Infiltrations Lymphomas Hodgkins disease Myeloproliferative syndromes Angiosarcomas Metastasis ( MC= Melanoma) Eosinophilic Granuloma Histiocytosis X Hamartomas Hemangioma Splenic cysts
  • 24. 4. Unknown Etiology Idiopathic splenomegaly Berylliosis Iron deficiencyanemia
  • 25. MASSIVE SPLENOMEGALY (>1000GM or >8cm) CML CLL Lymphoma Hairy cell leukemia Myelofibrosis with myeloid metaplasia Chronic malaria Kala - azar (Tropical Splenomegaly) Sarcoidosis Gaucher disease AIHA Diffuse splenic hemangiomatosis
  • 26. Moderate splenomegaly(4-8cm) Viral hepatitis Cirrhosis Lymphomas Amyloidosis Splenic abscess,infarct Hemolytic anemias IMN Hemochromatosis Polycythemias
  • 27. Mild splenomegaly (1-3cm) Acute malaria Typhoid kala-azar Septicemias SLE Infective endocarditis RA Thalassemia Minor Miliary TB Leptospirosis HIV CCF
  • 28. Step-wise approach to splenomegaly History Physical examination Laboratory tests Imaging Specialised tests
  • 29. History Mild vague, abdominal pain. Pain may be referred to the left shoulder. Early satiety from gastric displacement occurs with massive splenomegaly. Associated symptoms or signs Febrile illness (infectious) Pallor, dyspnea, bruising, and/or petechiae (hemolytic process) History of liver disease (congestive) Weight loss, constitutional symptoms (neoplastic) Pancreatitis (splenic vein thrombosis) Alcoholism, hepatitis (cirrhosis)
  • 30. Special situations associated with splenomegaly Fever -typhoid,malaria,kalaazar, infect.endocarditis, leukemia,lymphoma Tender spleen - rupture,abscess,infarct a/c illness + anemia- AIHA,leukemia Fever + LN- IMN, leukemia, lymhomas, SLE, sarcoid Anemia- hemolytic anemia, hemoglobinopathies Jaundice – cirrhosis, hemolytic anemia Pulsatile spleen- aneurysm High ESR-connective tissuedisorder Leukopenia- felty’s syndrome, septicemia
  • 31. Physical examination Size of the spleen Hepatomegaly Lymphadenopathy Fever Icterus Bruising,petechiae Oral & supf.sepsis Stigmata of liver disease Stigmata of RA/SLE Splinter hemorrhage,retinal hemorrhage Cardiac murmurs
  • 32. Lab investigations CBC Peripheral smear study Reticulocyte count Blood C/S Serology (viral, parasitic) LFT Hb electrophoresis / coombs test Coagulation profile Amylase/lipase AMA, Anti CCP ,RAfactor Bone marrow analysis
  • 33. Imaging USG CTscan sensitive & specificnon-invasive - etiology of splenomegaly - liver size,heterogenecity - splenic mets, abscess,calcf.,cysts - retro peritoneal LN - cranio caudal ln > 12cm Liver- spleen colloid scan- (RBC–Cr51,Tc99) - hepatic steatosis, SOL,splenic functions - PHT,colloid shift + MRI/ Doppler USG - portal / splenic veinthrombosis - cavernomas
  • 34. imaging MRI scanliver hemangiomas hemochromatosis erlenmeyer flask sign (Gaucher) PETscan Dx & staging of lymphomas determine metabolic cells in spleen
  • 35. Specialised testing Abdominal fat pad aspiration JAK-2 mutation Gene testing (bcr-abl ,C282Y) Enzyme testing Lymph node biopsy FNAC spleen Splenectomy Liver biopsy