Spleen Flashcards

1
Q

The splenic vessels run in which ligament?

A

the splenorenal

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2
Q

The short gastrics run in which ligament?

A

the gastrosplenic

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3
Q

T-cells take what architecture in the spleen?

A

periarterial lymphatic sheaths (PALS)

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4
Q

Howell-Jolly bodies are made of what?

A

nuclear remnants

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5
Q

What are pappenheimer bodies?

A

iron deposits in RBCs found in post-splenectomy patients

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6
Q

What are target cells?

A

immature RBCs

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7
Q

What are Heinz bodies?

A

intracellular denatured hemoglobin seen on a post-splenectomy blood smear

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8
Q

If you don’t find Howell-Jolly bodies after a splenectomy, what does this suggest?

A

the presence of an accessory spleen

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9
Q

What is the most reliable finding post-splenectomy on a blood smear?

A

Howell-Jolly bodies made up of nuclear remnants

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10
Q

Which hematologic disorders are indications for splenectomy?

A

ITP and spherocytosis

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11
Q

Angiographic intervention for splenic trauma should be considered for which patients?

A
  • those with greater than a grade 3 injury
  • those with a contrast blush
  • those with moderate hemoperitoneum
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12
Q

Describe the etiology and management of ITP.

A
  • thought to be secondary to glycoprotein IIb/IIIa auto-antibodies
  • initially managed medically with steroids and IVIG
  • can perform splenectomy for medically refractory patients, especially those with a good response to steroids
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13
Q

When do you transfuse platelets in a patient with ITP undergoing splenectomy?

A

after ligating the splenic artery if you can wait to prevent consumption

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14
Q

Describe the etiology, presentation, and treatment of hereditary spherocytosis.

A
  • due to an AD defect in cell membrane proteins like spectrum which make them less deformable and more likely to be culled by the spleen
  • presents with anemia and splenomegaly
  • splenectomy is indicated for symptomatic patients older than 6
  • often require cholecystectomy at the same time
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15
Q

Describe the etiology and management of splenic abscesses.

A
  • most due to IVDU, endocarditis, sickle cell disease, and infection of a traumatic pseudocyst
  • perc drains are appropriate for unilocular and thick walled lesions in stable patients
  • multi-locular and thin walled abscesses are suspicious for echinococal abscess and are indications for splenectomy
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16
Q

What is a well-defined hypodense splenic lesion most likely to be?

A

a splenic cyst

17
Q

What are the two types of splenic cysts?

A
  • pseudocysts (post-traumatic)
  • true cysts (parasitic, congenital, or neoplastic)
18
Q

How are splenic cysts managed?

A

laparoscopic resection or fenestration is indicated for cysts >5cm and those that are symptomatic

19
Q

What is the most common splenic tumor?

A

a hemangioma

20
Q

How are splenic hemangiomas managed?

A

with splenectomy if they become symptomatic

21
Q

What is the most common malignant tumor of the spleen?

A

angiosarcoma

22
Q

Angiosarcomas of the spleen are associated with what exposures?

A

vinyl chloride and thorium dioxide

23
Q

What is the most common lymphoma of the spleen, how is it managed surgically?

A
  • most common is CLL
  • indications for splenectomy are anemia and thrombocytopenia
24
Q

How are splenic artery aneurysms managed?

A
  • treated with >2cm and in all women of childbearing age given the high risk of rupture during pregnancy
  • typically treated endovascularly with coil embolization or covered stent
25
Q

What is the optimal timing for post-splenectomy vaccines?

A

2 weeks prior to elective splenectomy and at discharge or 2 weeks post-op

26
Q

How is OPSI initially managed?

A

if suspicious for OPSI, start antibiotics early before getting cultures

27
Q

When should you consider antibiotic prophylaxis against OPSI?

A

considered for patients under 10 but definitely not for adults

28
Q

What is the most common site of an accessory spleen? How else can it be found?

A
  • most commonly at the splenic hilum
  • can be found with a tagged RBC scan
29
Q

What is the most common organism associated with OPSI?

A

Strep pneumoniae

30
Q

What is the diagnosis for a patient with abdominal pain and CT showing the spleen in the RLQ with no flow in the splenic vein?

A
  • wandering spleen, caused by a lack of failure of the dorsal mesogastrium to fuse leading to a. lack of splenic ligaments
  • concerning for torsion and infarction
31
Q

What is the most common source of post-splenectomy bleeding?

A

the short gastrics

32
Q

If a splenectomy patient has lots of abdominal pain and a fluid collection in the lesser sac, what should be the concern? How is this managed?

A

pancreatic leak, managed with a perc drain

33
Q

What are the features of TTP?

A
  • fever
  • hemolytic anemia
  • renal failure
  • purpura
  • neurologic changes
34
Q

What is the etiology, presentation, and treatment for TTP?

A
  • due to defective ADAMTS13 metalloproteinase (cleaves vWF) leading to platelet aggregation in microvasculature
  • presents with fever, hemolytic anemia, renal failure, neurologic changes, and purpura
  • treated with plasmapharesis