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Spleen
Dr. Vivek Shrihari
Assistant Professor
Department of Surgery
MGMCRI, Puducherry
Contents:
• Anatomy
• Physiology (Functions)
• Splenic trauma
• Splenomegaly
Anatomy
• The Splenic tissue develops from condensations of mesoderm
in the dorsal mesogastrium.
• The weight of the normal adult spleen is 75–250 g.
• It 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 concave visceral surface lies in contact with these
structures, and the lower pole extends no further than the
mid-axillary line.
• There is a notch on the inferolateral border, and this may be
palpated when the spleen is enlarged.
Blood Supply:
• The tortuous splenic artery arises from the coeliac axis and
runs along the upper border of the body and tail of the
pancreas, to which it gives small branches.
• The short gastric and left gastroepiploic branches pass
between the layers of the gastrosplenic ligament.
• The main splenic artery generally divides into superior and
inferior branches, which, in turn, subdivide into several
segmental branches.
• The splenic vein is formed from several tributaries that drain
the hilum.
• The vein runs behind the pancreas, receiving several small
tributaries from the pancreas before joining the superior
mesenteric vein at the neck of the pancreas to form the
portal vein.
• The splenic pulp is invested by an external serous and
internal fibroelastic coat which is reflected inwards at the
hilum onto the vessels to form vascular sheaths.
• The lymphatic drainage comprises efferent vessels in the
white pulp that run with the arterioles and emerge from
nodes at the hilum.
• These nodes and lymphatics drain via retropancreatic nodes
to the coeliac nodes.
• Sympathetic nerve fibres run from the coeliac plexus and
innervate splenic arterial branches.
Functions of the Spleen
• Although the spleen was previously thought to be
dispensable, increasing knowledge of its function has led to a
conservative approach in the management of conditions
involving the spleen.
• It is now recognized that an incidental splenectomy during
the course of another operative procedure increases the risk
of complication and death.
• The surgeon should therefore normally endeavor to preserve
the spleen to maintain the following functions:
Immune function:
• The spleen processes foreign antigens and is the major site of
specific immunoglobulin M (IgM) production.
• The non-specific opsonins, properdin and tuftsin, are
synthesized.
• These antibodies are of B- and T-cell origin and bind to the
specific receptors on the surface of macrophages and
leukocytes, stimulating their phagocytic, bactericidal and
tumoricidal activity.
Filter function:
• Macrophages in the reticulum capture cellular and non-
cellular material from the blood and plasma.
• This will include the removal of effete platelets and red blood
cells.
• This process takes place in the sinuses and the splenic cords
by the action of the endothelial macrophages.
• Iron is removed from the degraded hemoglobin during red
cell breakdown and is returned to the plasma.
• Removed non-cellular material may include bacteria and, in
particular, pneumococci.
Pitting:
• Particulate inclusions from red cells are removed, and the
repaired red cells are returned to the circulation.
• These include Howell–Jolly and Heinz bodies, which
represent nuclear remnants and precipitated hemoglobin or
globin subunits, respectively.
Reservoir function:
• This function in humans is less marked than in other species,
but the spleen does contain approximately 8 per cent of the
red cell mass.
• An enlarged spleen may contain a much larger proportion of
the blood volume.
Cytopoiesis:
• From the fourth month of intrauterine life, some degree of
hemopoiesis occurs in the fetal spleen.
• Stimulation of the white pulp may occur following antigenic
challenge, resulting in the proliferation of T and B cells and
macrophages.
• This may also occur in myeloproliferative disorders,
thalassaemias and chronic haemolytic anaemias.
Splenic Trauma
• Spleen is the most common organ to be injured in abdominal
trauma.
• Etiology of trauma:
Closed trauma: Direct, Indirect, & Spontaneous
Open trauma: Gun-shots, Puncture, & Iatrogenic (e.g.
Gastrectomy)
Pathology & Grades:
Description
Class 1 Sub-capsular hematoma
Class 2 Superficial tears
Class 3 Deep tears
Class 4 Avulsion of pole of spleen
Class 5 Complete depulping of spleen
Class 6 Injury of a vascular pedicle
Clinical types of rupture spleen:
Fatal Delayed Classic
Classic Presentation of Rupture Spleen
Initial shock  Lucid interval  Internal hemorrhage
STAGE OF SHOCK
GENERAL: Tachycardia, Hypotension, Hypothermia, Decreased urine output
LOCAL:
• Inspection: Ecchymosis, Bruises, Fracture of ribs, Abdominal distention
• Palpation: Rigidity, Tenderness, Rebound tenderness
• Percussion: Shifting dullness
• Auscultation: Diminished intestinal sounds
• DRE: Fullness in retro-vesical pouch, Douglass pouch
Special signs:
• Kehr’ Sign: Referred pain in Lt shoulder , hyperesthesia form
diaphragmatic irritation
• Balance sign: Shifting dullness on Right side (free blood) +
Fixed Dullness on Left side (clots, hematoma)
• Cullen’s sign: (late) Bluish discoloration around the umbilicus
Investigations:
• U/S & CT scan show hematoma, free peritoneal bleeding..
U/S, CT replaced "DIAGNOSTIC PERITONEAL LAVAGE" (used
when there's no time)
• Arteriography (diagnostic & therapeutic)
• Plain x-ray: elevated left copula of diaphragm + indentation
of fundic air bubble + Obliteration of Lt. psoas shadow
• Laboratory: CBC, KFTs, FBS, Electrolytes
Fatal Type
Dies within short period:
• Grade 4 or 5.
• Severely Shocked.
• Associated with other visceral injury.
Delayed Type
Initial shock  Long lucid interval up to 15 days  Internal
hemorrhage
This delay is due to:
• Sub-capsular hematoma that may rupture later
• The omentum seals the tear then retracts later
• Blood clot seals the vessel then dislodges when Bl.P. rises.
Treatment
This patient is a POLYTRAUMAIIZED PATIENT So
RESUSCITATION AND MONITORIG
Then According to:
• ln adults: urgent laparotomy & Splenectomy
• In children:
l) Splenic preservation: (Total or Partial splenectomy, Splenic A. ligation, or
Embolization)
2) Vaccination: (pneumococcal)
3) Post operative penicillin
Recently: Splenic preservation even in adults.
Splenomegaly
• Splenomegaly is a common feature of many disease processes
• It should be borne in mind, however, that many conditions
affecting the spleen, such as idiopathic thrombocytopenic
purpura, may be associated with enlargement, but the gland
is seldom palpable.
• Few conditions that cause splenomegaly will require
splenectomy as part of treatment.
Hypersplenism
It is an indefinite clinical syndrome that is characterized by:
• splenic enlargement, and
• any combination of: anaemias, leukopenia or
thrombocytopenia, with compensatory bone marrow
hyperplasia and
• improvement after splenectomy.
Careful clinical judgement is required to balance the long- and
short-term risks of splenectomy against continued conservative
management.
Thank You !

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Spleen

  • 1. Spleen Dr. Vivek Shrihari Assistant Professor Department of Surgery MGMCRI, Puducherry
  • 2. Contents: • Anatomy • Physiology (Functions) • Splenic trauma • Splenomegaly
  • 3. Anatomy • The Splenic tissue develops from condensations of mesoderm in the dorsal mesogastrium. • The weight of the normal adult spleen is 75–250 g. • It 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 concave visceral surface lies in contact with these structures, and the lower pole extends no further than the mid-axillary line. • There is a notch on the inferolateral border, and this may be palpated when the spleen is enlarged.
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  • 9. Blood Supply: • The tortuous splenic artery arises from the coeliac axis and runs along the upper border of the body and tail of the pancreas, to which it gives small branches. • The short gastric and left gastroepiploic branches pass between the layers of the gastrosplenic ligament. • The main splenic artery generally divides into superior and inferior branches, which, in turn, subdivide into several segmental branches.
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  • 11. • The splenic vein is formed from several tributaries that drain the hilum. • The vein runs behind the pancreas, receiving several small tributaries from the pancreas before joining the superior mesenteric vein at the neck of the pancreas to form the portal vein.
  • 12. • The splenic pulp is invested by an external serous and internal fibroelastic coat which is reflected inwards at the hilum onto the vessels to form vascular sheaths. • The lymphatic drainage comprises efferent vessels in the white pulp that run with the arterioles and emerge from nodes at the hilum. • These nodes and lymphatics drain via retropancreatic nodes to the coeliac nodes. • Sympathetic nerve fibres run from the coeliac plexus and innervate splenic arterial branches.
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  • 14. Functions of the Spleen • Although the spleen was previously thought to be dispensable, increasing knowledge of its function has led to a conservative approach in the management of conditions involving the spleen. • It is now recognized that an incidental splenectomy during the course of another operative procedure increases the risk of complication and death. • The surgeon should therefore normally endeavor to preserve the spleen to maintain the following functions:
  • 15. Immune function: • The spleen processes foreign antigens and is the major site of specific immunoglobulin M (IgM) production. • The non-specific opsonins, properdin and tuftsin, are synthesized. • These antibodies are of B- and T-cell origin and bind to the specific receptors on the surface of macrophages and leukocytes, stimulating their phagocytic, bactericidal and tumoricidal activity.
  • 16. Filter function: • Macrophages in the reticulum capture cellular and non- cellular material from the blood and plasma. • This will include the removal of effete platelets and red blood cells. • This process takes place in the sinuses and the splenic cords by the action of the endothelial macrophages. • Iron is removed from the degraded hemoglobin during red cell breakdown and is returned to the plasma. • Removed non-cellular material may include bacteria and, in particular, pneumococci.
  • 17. Pitting: • Particulate inclusions from red cells are removed, and the repaired red cells are returned to the circulation. • These include Howell–Jolly and Heinz bodies, which represent nuclear remnants and precipitated hemoglobin or globin subunits, respectively.
  • 18. Reservoir function: • This function in humans is less marked than in other species, but the spleen does contain approximately 8 per cent of the red cell mass. • An enlarged spleen may contain a much larger proportion of the blood volume.
  • 19. Cytopoiesis: • From the fourth month of intrauterine life, some degree of hemopoiesis occurs in the fetal spleen. • Stimulation of the white pulp may occur following antigenic challenge, resulting in the proliferation of T and B cells and macrophages. • This may also occur in myeloproliferative disorders, thalassaemias and chronic haemolytic anaemias.
  • 20. Splenic Trauma • Spleen is the most common organ to be injured in abdominal trauma. • Etiology of trauma: Closed trauma: Direct, Indirect, & Spontaneous Open trauma: Gun-shots, Puncture, & Iatrogenic (e.g. Gastrectomy)
  • 21. Pathology & Grades: Description Class 1 Sub-capsular hematoma Class 2 Superficial tears Class 3 Deep tears Class 4 Avulsion of pole of spleen Class 5 Complete depulping of spleen Class 6 Injury of a vascular pedicle
  • 22. Clinical types of rupture spleen: Fatal Delayed Classic
  • 23. Classic Presentation of Rupture Spleen Initial shock  Lucid interval  Internal hemorrhage STAGE OF SHOCK GENERAL: Tachycardia, Hypotension, Hypothermia, Decreased urine output LOCAL: • Inspection: Ecchymosis, Bruises, Fracture of ribs, Abdominal distention • Palpation: Rigidity, Tenderness, Rebound tenderness • Percussion: Shifting dullness • Auscultation: Diminished intestinal sounds • DRE: Fullness in retro-vesical pouch, Douglass pouch
  • 24. Special signs: • Kehr’ Sign: Referred pain in Lt shoulder , hyperesthesia form diaphragmatic irritation • Balance sign: Shifting dullness on Right side (free blood) + Fixed Dullness on Left side (clots, hematoma) • Cullen’s sign: (late) Bluish discoloration around the umbilicus
  • 25. Investigations: • U/S & CT scan show hematoma, free peritoneal bleeding.. U/S, CT replaced "DIAGNOSTIC PERITONEAL LAVAGE" (used when there's no time) • Arteriography (diagnostic & therapeutic) • Plain x-ray: elevated left copula of diaphragm + indentation of fundic air bubble + Obliteration of Lt. psoas shadow • Laboratory: CBC, KFTs, FBS, Electrolytes
  • 26. Fatal Type Dies within short period: • Grade 4 or 5. • Severely Shocked. • Associated with other visceral injury.
  • 27. Delayed Type Initial shock  Long lucid interval up to 15 days  Internal hemorrhage This delay is due to: • Sub-capsular hematoma that may rupture later • The omentum seals the tear then retracts later • Blood clot seals the vessel then dislodges when Bl.P. rises.
  • 28. Treatment This patient is a POLYTRAUMAIIZED PATIENT So RESUSCITATION AND MONITORIG Then According to: • ln adults: urgent laparotomy & Splenectomy • In children: l) Splenic preservation: (Total or Partial splenectomy, Splenic A. ligation, or Embolization) 2) Vaccination: (pneumococcal) 3) Post operative penicillin Recently: Splenic preservation even in adults.
  • 29. Splenomegaly • Splenomegaly is a common feature of many disease processes • It should be borne in mind, however, that many conditions affecting the spleen, such as idiopathic thrombocytopenic purpura, may be associated with enlargement, but the gland is seldom palpable. • Few conditions that cause splenomegaly will require splenectomy as part of treatment.
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  • 31. Hypersplenism It is an indefinite clinical syndrome that is characterized by: • splenic enlargement, and • any combination of: anaemias, leukopenia or thrombocytopenia, with compensatory bone marrow hyperplasia and • improvement after splenectomy. Careful clinical judgement is required to balance the long- and short-term risks of splenectomy against continued conservative management.
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