LOOKED UP REVIEWS Flashcards

1
Q

algorithm for gastrinoma workup: initial, labs values, imaging

A

initial:
fasting serum gastrin level 72 hours off PPIs
(not definitive diagnosis)

Baseline gastrin level nondiagnostic

All patient’s require secretary stimulation test to confirm:
Most widely used level 200
Recent recommendations 110-120

Imaging:
Somatostatin scintigraphy greater sensitivity than all conventional studies combined

EUS high-sensitivity for detection of pancreatic gastrinoma

Not good for duodenal gastrinoma (even intraop)

If cannot find gastrinoma:
Hepatic vein sampling with calcium stimulation

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2
Q

arcuate line of the abdomen, other names, relationships to rectus, internal oblique, transversus, external landmarks, epigastric vessels,

A

also called linea semicircularis or Douglas’ line

Horizontal lower limit of the posterior (lateral) layer of the rectus sheath
(Above you have two layers of fascia to close)

1/3 of the distance from the umbilicus to the pubic crest

where the inferior epigastric vessels perforate the rectus abdominis.

Inferior to the arcuate line, the internal oblique and transversus abdominis aponeuroses merge and pass superficial (i.e. anteriorly) to the rectus muscle.

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3
Q

The linea semilunaris

A

a curved tendinous line placed one on either side of the rectus abdominis boarding the lateral edges of the rectus muscle

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4
Q

Acinic cell carcinoma of the parotid treatment

A

malignant
“En bloc surgical resection”-does not include facial nerve if no invasion

superficial parotidectomy with radiation and mass confined to superficial parotid

total parotidectomy deep lobe involved

 radiation used when:
 unclear margin- partial parotidectomy to spare facial nerve
High-grade
Neural invasion
Invasion of surrounding structures
Metastatic
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5
Q

small bowel lymphoma most common type and site

A

Most common non-Hodgkin’s:
diffuse
B cell
MALT lymphoma

most common site of non-Hodgkin’s:
Ileum-large immune component

in children younger than 10 years, lympomas are the most common intestinal neoplasm

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6
Q

most common GI site of lymphoma

A

stomach

Second most-small bowel

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7
Q

risk factors for small bowel lymphoma

A

celiac - Non-Hodgkin’s T-cell lymphoma

HIV-aggressive B-cell lymphoma

H. pylori-MALT

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8
Q

diagnosis small bowel lymphoma

A

CT scan

Tissue biopsy

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9
Q

treatment small bowel lymphoma, early stage, symptomatic, cell type tx is

A

local early stage:
surgical resection all gross disease prevents perforation/obstruction (Cam)

in the absence of symptoms:
may respond to chemotherapy without the need for surgery (Sab)!

B cell lymphomas:
more chemosensitive have high remission rates with or without surgery.

T cell lymphomas:
traditionally more resistant to therapy and will progress to symptoms of obstruction or perforation if not resected.

resection is indicated:
at any onset of symptoms regardless of type
because progression to life-threatening hemorrhage or perforation with worse prognosis

Advanced disseminated:
Surgery only for tissue biopsy and possibly pale eating complications

Chemotherapy-test for diffuse large cell

Anaplastic resistant to chemotherapy and

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10
Q

most common site of GIST tumor in small bowel

A

duodenum (2nd portion) to- this is from H. pylori risk factor in stomach/duodenum

careful, lymphomas most common ileum

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11
Q

diagnosis gist tumor and small bowel

A

NO biopsy

CT scan abdomen pelvis

Smooth well-circumscribed exophytic growth
Large tumor-central necrosis/hemorrhage

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12
Q

Treatment of GIST tumor small bowel

A

localized disease:
complete gross resection With intact capsule
en bloc resection of involved organs

Involved periampullary tumors:
May require Whipple

NO lymphadenectomy -

metatarsal metastasis to liver

marginal resectable tumors:
Neoadjuvant Imatinib

adjuvant for:
incomplete resection
Recurrent disease
Metastatic disease

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13
Q

von Willebrand disease mechanism

A

deficient von Willebrand factor

Cannot link platelets on collagen on endothelium

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14
Q

treatment of von Willebrand’s 1, 2, 3

A
II:
Low circulating level
DDAVP
Conjugated estrogens
 von Willebrand factor
Cryoprecipitate

II:
Qualitative - may not work to give DDAVP because of defective present von Willebrand factor
von Willebrand factor
Cryoprecipitate

 III:
Complete absence of production
Associated with low factor a level
 severe bleeding -  like hemophilia A.
 DDAVP will not work
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15
Q

unresectable pancreatic cancer

A
Vascular-
 circumferential encasement or invasion or inclusion of:
Portal vein
Superior mesenteric vein
Superior mesenteric artery

exception may be made for venous structure- SMV, portal vein

 advanced disease:
Extension beyond pancreas capsule and the retroperitoneum
Neural
Nodes outside direct field of resection:
Pubic access
Superior mesenteric artery
Hepatoduodenal ligament
 frank metastases:
Liver
Peritoneal

careful, pancreatic metastases to not undergo meniscectomy peek and shreek

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16
Q

blood products associated with TRALI and mechanism

A

RBC
Platelet
Plasma!

the DONOR antibodies of attach host leukocyte

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17
Q

Workup of a patient with suspected Cushing’s syndrome includes

A
24-hour urine cortisol,
late evening salivary cortisol, 
ACTH level, 
high dose dexamethasone suppression test, 
MRI head, 
CT chest/abdomen/pelvis, 
inferior petrosal sinus sampling.
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18
Q

treatment of melanoma

A

in situ:
0.5-1 cm excision

less than 1 mm:
1 cm excision

1 and greater mm:
2 cm excision!

1-2 mm - 1 cm margin maybe acceptable if greater excision would cause significant morbidity

 sentinel node:
1  millimeter or greater
 ulceration
Regression
Absence of clinical note
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19
Q

basal cell carcinoma margin

A
low risk:
 4-5 mm
 less than 2 cm trunk/extremities
Head and neck less than 1 cm
Less than 6 mm-  face, feet, hands
 High-risk:
 1 cm
 size greater than 6 mm
Recurrent
Immunocompromised
Radiation field
Sclerosing
Micronodular
Perineural invasion
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20
Q

squamous cell carcinoma skin margin

A

same his basal

 low risk:
 4-5 mm
 less than 2 cm trunk/extremities
Head and neck less than 1 cm
Less than 6 mm-  face, feet, hands
 High-risk:
 1 cm
Recurrent
Immunocompromised
Radiation field
Sclerosing
Micronodular
Perineural invasion
 also:
Poorly differentiated
Adenoid
Adenosquamous
Desmoplastic
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21
Q

most common skin cancer and

A

Basal cell

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22
Q

second most common skin cancer

A

squamous cell

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23
Q

Merkel cell carcinoma skin, risk factors, Workup, treatment

A

immunocompromise
polyomavirus

CT scan

Excision down to fascia or pericranium:
1.5-2 cm margin

sentinel node or no dissection

adjuvant radiation
chemotherapy for regional or distant metastases

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24
Q

dermatofibroma sarcoma protuberans

A

30-40-year-old

Wide excision with frozen section
3 cm margin
Or
Mohs

radiation for colon
Less than 1 cm margin
Involved margin
Or cannot reexcised

25
Q

treatment of Kaposi’s sarcoma the skin workup, treatment

A

chest x-ray and fecal occult rules out systemic solid organ

optimize antiretrovirals and immune status

Initial treatment for local disease:
Chemotherapy-vinblastine
or
Radiation

systemic disease
Doxorubicin

26
Q

angiosarcoma Skin

A

head and neck elderly

treatment:
2 cm margin used to require his free flap

Adjuvant:
Postoperative radiation

metastases to the lungs

advanced disease on presentation: the
chemotherapy

27
Q

Central DI will presentation and treatment

A

traumatic brain injury.

aantidiuretic hormone (ADH) synthesis is disrupted due to injury of the hypothalamus or pituitary

leads to an inability to concentrate urine and a decrease in the urine osmolarity.

cause excessive urine output,

can be treated with desmopressin.

ADH replacement in the form of desmopressin.

28
Q

Peripheral DI

A

defect in the ADH receptors at the level of the kidney.

will not respond to desmopressin

29
Q

most common organism in pathogenic liver abscess

A

gallbladder source :
Escherichia coli
Klebsiella

Other organisms:
Staphylococcus
Streptococcus
Enterococcus (careful, different than Enterobacter)
Bacteroides
30
Q

esophageal perforation workup

A

chest x-ray:
hydropneumothorax

barium swallow for chest
Gastrografin for abdomen

most perforations:
Above the GE junction on LEFT

endoscopy if swallow negative
or if surgery planned

31
Q

Boerhaave syndrome Mechanism

A

disruption of normal vomiting reflux that because the sphincter relaxation

Increase intrathoracic esophageal pressure

32
Q

findings consistent with mucosal injury the esophagus

A

blood
Because the hematoma
Flap
Esophagus difficult to insufflate

33
Q

treatment of esophageal perforation

A

stabilize:
No NG tube and a management decision planned

contained perforation:
N.p.o., antibiotics, observation
temporary endoluminal stent may be placed and removed 6-12 weeks
with followup swallow or scope

unstable patient with contained perforation:
Stent may be entertained

 unstable patient with free perforation:
Surgery
Upper two thirds: rglht thoracotomy
 lower  one third:  left thoracotomy
 GE junction:  Left thoracotomy /  upper midline abdominal

cannot identify perforation:
Drainage

 inflammation Without distal obstruction:
 primary repair
Muscle flap
Drainage
J-tube
 inflammation with distal obstruction:
 resection/exclusion
  esophagostomy
 drainage
J-tube
G-tube
 no inflammation with distal obstruction:
 resection
RECONSTRUCTION
 drainage
J-tube

no inflammation no obstruction:
Primary repair
Muscle flap
Drainagel

34
Q

4 underlying conditions that mandates esophagectomy even without inflammation with free perforation of the esophagus

A

End-stage achalasia - Megaesophagus
cancer - resectable
caustic injury
severe peptic stricture

35
Q

management of small cervical perforation

A

drainage only-difficult to locate

36
Q

surgical landmarks the finding esophagus into thirds

A

carina and above - fourth intercostal space right

Mid esophageal perforation-sixth intercostal space right

lower esophageal - seventh intercostal space left

37
Q

most narrow portions of the esophagus at risk for perforation

A

cricopharyngeus muscle is the narrowest point of the gastrointestinal tract

aortic arch - left mainstem bronchus and aorta abut the esophagus, the bronchoaortic constriction at the level of the fourth thoracic vertebra

diaphragmatic constriction

38
Q

recommendations antibiotic prophylaxis for children after splenectomy

A

prophylaxis with penicillin is routinely practiced in children, at least during the first 2 postsplenectomy
Sab

39
Q

and test results for TTP versus ITP

A

negative for TTP

Careful, positive for ITP

40
Q

management of Hodgkin’s lymphoma

A

NO staging splenectomy

Treatment chemotherapy

Splenectomy if:
Thrombocytopenia symptoms of splenomegaly l

41
Q

findings and staging theof Hodgkin’s lymphoma

A

Reed-Sternberg cells: disease or B cells
staging:
1 single node
2 chest/mediastinum - can be bilateral
3 both sides the diaphragm
4 extranodal involvement (careful, spleen counts this lymph node)
bone marrow count is metastasis to

LEpstein-Barr virus

42
Q

ITP and children

A

usually self-limiting

Associated with previous infectious illness

Observation short-term medical therapy

IVIG his risk of intracranial hemorrhage when platelet counts below 20,000 short term prednisone

Splenectomy reserved if thrombocytopenia greater than one year

Fails medical management

Severe thrombocytopenia

life-threatening bleed presentation

43
Q

treatment of ITP medical

A

is glucocorticoid administration (typically, prednisone

less than 50,000/mm3 and symptoms such as mucous membrane bleeding, high-risk conditions (e.g., active lifestyle, hypertension, peptic ulcer disease)

20,000 to 30,000/mm3, even without symptoms,

IV immunoglobulin is important for the treatment of acute bleeding, in pregnancy, or for patients being prepared for operation, including splenectomy.

Platelet transfusion is indicated only for those who experience severe hemorrhage.

44
Q

treatment ITP surgical

A

severe thrombocytopenia, with counts less than 10,000 for 6 weeks or longer,

thrombocytopenia refractory to glucocorticoid treatment,

require toxic doses of steroid to achieve remission

severe thrombocytopenia, with counts less than 10,000/mm3 for 6 weeks or longer, those with thrombocytopenia refractory to glucocorticoid treatment, or those who require toxic doses of steroid to achieve remission, the treatment of choice is to proceed to splenectomy.

pregnant in the second trimester of pregnancy who have also failed steroid treatment or IV Ig therapy with platelet counts less than 10,000/mm3 without symptoms
or
less than 30,000/mm3 with bleeding problems

45
Q

hereditary spherocytosis

A

Splenectomy is indicated in cases of severe anemia with these conditions, except hereditary xerocytosis, which results in only mild anemia of limited clinical significance.

normalization of the erythrocyte morphology does not occur

Splenectomy should be delayed until the age of 5 years to preserve immunologic function of the spleen and reduce the risk of OPSI.

Diagnosis is made by examination of a peripheral blood smear, increased reticulocyte count, increased osmotic fragility, and a negative Coombs’ test.

46
Q

treatment of Hereditary elliptocytosis, hereditary pyropoikilocytosis, hereditary xerocytosis, and hereditary hydrocytosis

A

Splenectomy is indicated in cases of severe anemia with these conditions,

except hereditary xerocytosis, which results in only mild anemia of limited clinical significance.

47
Q

treatment of G6PD deficiency

A

Primary treatment, therefore, is avoidance of exacerbation

splenectomy is rarely indicated. T

his X-linked condition is typically seen in people of African, Middle Eastern, or Mediterranean ancestry. Hemolytic anemia in these patients most often occurs after infection or exposure to certain foods, medications, or chemicals. cerbation of the condition.

48
Q

when his splenectomy indicated for sickle cell and thalassemia

A

Hypersplenism and acute splenic sequestration are life-threatening disorders in children with thalassemia and sickle cell disease. I

Resuscitation with hydration and transfusion may be followed by splenectomy in these patients.

49
Q

Hypersplenism and acute splenic sequestration presentation of sickle cell thalassemia

A

apid splenic enlargement, which results in severe pain and may require multiple blood transfusions. Patients with acute splenic sequestration crisis present with severe anemia, splenomegaly, and an acute bone marrow response, with erythrocytosis.

50
Q

Splenic abscesses with sickle cell anemia

A

fever, abdominal pain, and a tender enlarged spleen.

leukocytosis, as well as thrombocytosis and Howell-Jolly bodies indicating a functional asplenia.

Salmonella and Enterobacter spp. and other enteric organisms are commonly seen in those with a splenic abscess.

resuscitation and may require urgent splenectomy

51
Q

management of Hodgkin’s lymphoma when is staging laparotomy indicated

A

rarely

Staging laparotomy remains appropriate for select patients:
arly clinical disease stages (IA or IIA) in whom abdominal staging will significantly alter therapeutic management.

52
Q

treatment of Hodgkin’s lymphoma

A

Early-stage Hodgkin’s
RADIATION cured therapy alone.

advance disease:
Chemotherapy

relapse
intra-abdominal involvement
B symptoms

53
Q

when is splenectomy indicated for non-Hodgkin’s lymphoma

A

consider first-line treatment if splenic marginal zone lymphoma-indolent B-cell lymphoma-old her presentation-usually isolated spleen

and for

massive splenomegaly leading to
abdominal pain,
early satiety,
fullness.

It may also be indicated for:
anemia,
neutropenia,
thrombocytopenia associated with hypersplenism.

54
Q

treatment for leukemia of the spleen

A

chemotherapy

Splenectomy rarely indicated-
Pancytopenia
Refractory to medical therapy
Splenic rupture
Severe bleeding from thrombocytopenia
55
Q

splenic chronic lymphocytic leukemia

A

B cell

50-year-old plus

Bone marrow transplantation currently offers the only known cure for CLL. Splenectomy is indicated for patients with refractory splenomegaly and pancytopenia, which results in improvements in blood counts in 60% to 70% of patients.[21] the

splenectomy and symptomatic
including thrombocytopenia

splenectomy a worse outcome if advanced and refractory to medical management

56
Q

chronic myelogenous leukemia spleen

A

first line treatment is Imatinib Gleevec! - transplantation less common.

splenectomy if hypersplenism - but not survival benefit in an early chronic phase or before bone transplant

57
Q

primary myelofibrosis myeloid metaplasia

A

hyperplasia of normal myeloid precursor cells with pulmonary fibrosis and extramedullary hematopoiesis

risk factor radiation toxic industrial chemicals

Splenectomy for colon
Symptoms including hemolysis, transfusions, splenic infarctions, portal hypertension, refractory variceal hemorrhage

Caution-substantial risk of morbidity and mortality

Splenectomy also considered for delineation

58
Q

Treatment of splenic abscesses

A

depends on whether the abscess is unilocular or multilocular.

Unilocular abscesses are often amenable to percutaneous drainage, along with antibiotics,[29] with success rates reported at 75% to 90% for unilocular lesions. Multilocular lesions, however, are usually treated with splenectomy, drainage of the left upper quadrant, and antibiotics

59
Q

wandering spleen

A

choosing splenopexy or splenectomy.[32]