Spleen and Splenectomy, C60 P458-463 Flashcards

(45 cards)

1
Q

Which arteries supply the
spleen?
P458

A
Splenic artery (a branch of the celiac
trunk) and the short gastric arteries that
arise from the gastroepiploic arteries
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2
Q

What is the venous drainage
of the spleen?
P458

A

Portal vein, via the splenic vein and the

left gastroepiploic vein

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3
Q

What is said to “tickle” the
spleen?
P459

A

Tail of the pancreas

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4
Q

What percentage of people
have an accessory spleen?
P459

A

≈20%

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5
Q

What percentage of the total
body platelets are stored in
the spleen?
P459

A

33%

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6
Q

What are the functions of
the human spleen?
P459

A
Filters abnormal RBCs (does NOT store
RBCs like canine spleen!), stores platelets,
produces tuftsin and properdin (opsins),
produces antibodies (especially IGM) and
is site of phagocytosis
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7
Q

What is “delayed splenic
rupture”?
P459

A
Subcapsular hematoma or
pseudoaneurysm may rupture some time
after blunt trauma, causing “delayed
splenic rupture”; rupture classically
occurs about 2 weeks after the injury and
presents with shock/abdominal pain
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8
Q

What are the signs/symptoms
of ruptured/injured spleen?
P459

A

Hemoperitoneum and Kehr’s sign, LUQ

abdominal pain, Ballance’s sign

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9
Q

What is Kehr’s sign?

P459

A

Left shoulder pain seen with splenic

rupture

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10
Q

What is Ballance’s sign?

P459

A

LUQ dullness to percussion

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11
Q

What is Seagesser’s sign?

P459

A

Phrenic nerve compression causing neck

tenderness in splenic rupture

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12
Q

How is a spleen injury
diagnosed?
P459

A

Abdominal CT, if the patient is stable;
DPL or FAST exam if the patient is
unstable

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13
Q

What is the treatment?

P459

A
1. Nonoperative in a stable patient with
    an isolated splenic injury without hilar
    involvement/complete rupture
2. If patient is unstable, DPL/FAST
    laparotomy with splenorrhaphy or
    splenectomy
3. Embolization is an option in selected
    patients
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14
Q

What is a splenorrhaphy?

P460

A

Splenic salvage operation: wrapping vicral
mesh, aid of topical hemostatic agents or
partial splenectomy, sutures (buttressed)

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15
Q

What are the other
indications for splenectomy:
Malignant diseases?
P460

A
Hodgkin’s staging not conclusive by CT
    scan (rare)
Splenic tumors (primary/metastatic/
    locally invasive)
Hypersplenism caused by other
    leukemias/non-Hodgkin’s lymphomas
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16
Q

What are the other
indications for splenectomy:
Anemias?
P460

A
Medullary fibrosis with myeloid
    metaplasia
Hereditary elliptocytosis
Sickle cell anemia (rare, most
    autosplenectomize)
Pyruvate kinase deficiency
Autoimmune hemolytic anemia
Hereditary spherocytosis
Thalassemias (e.g., 	ℬ-thalassemia major
    a.k.a. Cooley’s)
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17
Q

What are the other
indications for splenectomy:
Thrombocytopenia?
P460

A

ITP (Idiopathic Thrombocytopenic
Purpura)
TTP (Thrombotic Thrombocytopenic
Purpura)

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18
Q

What are the other
indications for splenectomy:
Miscellaneous indications?
P460

A

Variceal bleeding with splenic vein
thrombosis, Gaucher’s disease, splenic
abscess, refractory splenic cysts,
hypersplenism, Felty’s syndrome

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19
Q

Is G6PD deficiency an
indication for splenectomy?
P460

20
Q

What are the possible
postsplenectomy
complications?
P460

A

Thrombocytosis, subphrenic abscess,
atelectasis, pancreatitis gastric dilation,
and Overwhelming PostSplenectomy
Sepsis (OPSS)

21
Q

What causes OPSS?

P460

A

Increased susceptibility to fulminant
bacteremia, meningitis, or pneumonia
because of loss of splenic function

22
Q

What is the incidence of
OPSS in adults?
P461

23
Q

What is the incidence and
overall mortality of OPSS in
children?
P461

A

1% to 2% with 50% mortality rate

24
Q

What is the typical
presentation of OPSS?
P461

A

Fever, lethargy, common cold, sore
throat, URI followed by confusion, shock,
and coma with death ensuing within 24
hours in up to 50% of patients

25
What are the common organisms associated with OPSS? P461
Encapsulated: Streptococcus pneumoniae, Neisseria meningitides, H. influenzae
26
What is the most common bacteria in OPSS? P461
Streptococcus pneumoniae
27
What is the preventive treatment of OPSS? P461
``` Vaccinations for pneumococcus, H. influenzae, and meningococcus Prophylactic penicillin for all minor infections/illnesses and immediate medical care if febrile illness develops ```
28
What is the best time to give immunizations to splenectomy patients? P461
Preoperatively, if at all possible If emergent, then 2 weeks postoperatively
29
What lab tests are abnormal after splenectomy? P461
WBC count increases by 50% over the baseline; marked thrombocytosis occurs; RBC smear is abnormal
30
What are the findings on postsplenectomy RBC smear? P461
Peripheral smear will show Pappenheimer bodies, Howell-Jolly bodies, and Heinz bodies
31
When and how should thrombocytosis be treated? P461
When platelet count is > 1 million, most | surgeons will treat with aspirin
32
What is the most common cause of splenic vein thrombosis? P461
Pancreatitis
33
What opsonins does the spleen produce? P461
PROperdin, TUFtsin (Think: | “PROfessionally TUF spleen”)
34
What is the most common cause of ISOLATED GASTRIC varices? P462
Splenic vein thrombosis (usually from | pancreatitis)
35
What is the treatment of gastric varices caused by splenic vein thrombosis? P462
Splenectomy
36
Which patients develop hyposplenism? P462
Patients with ulcerative colitis
37
What vaccinations should every patient with a splenectomy receive? P462
Pneumococcus Meningococcus Haemophilus influenzae type B
38
Define hypersplenism. | P462
``` Hyperfunctioning spleen Documented loss of blood elements (WBC, Hct, platelets) Large spleen (splenomegaly) Hyperactive bone marrow (trying to keep up with loss of blood elements) ```
39
Define splenomegaly. | P462
Enlarged spleen
40
What is idiopathic thrombocytopenic purpura (ITP)? P462
Autoimmune (antiplatelet antibodies IgG in 90% of patients) platelet destruction leading to troublesome bleeding and purpura
41
``` What is the most common cause of failure to correct thrombocytopenia after splenectomy for ITP? P462 ```
Missed accessory spleen
42
What are the “I’s” of ITP? | P462
``` Immune etiology (IgG antiplatelets ABs) Immunosuppressive treatment (initially treated with steroids) Immune globulin Improvement with splenectomy (75% of patients have improved platelet counts after splenectomy) ```
43
What is TTP? | P462
Thrombotic Thrombocytopenic Purpura
44
What is the treatment of choice for TTP? P463
Plasmapheresis (splenectomy reserved as | a last resort—very rare)
45
What is the most common physical finding of portal hypertension? P463
Splenomegaly