Retroperitoneal Pathology Ch 16 Flashcards

1
Q

Adrenal cortical syndromes..

A
  • Addison’s disease
  • adrenogenital syndrome/adrenal virilism
  • Conn’s syndrome (aldosteronism)
  • Cushing’s syndrome
  • Waterhouse-Friderishsen syndrome
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2
Q
  • affects males and females equally
  • adrenocortical insufficiency
    • hyopfunction of adrenal gland**
    • atrophy of the adrenal cortex with decreased production of cortisol and sometimes aldosterone
A

Addison’s disease

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3
Q

causes and examples of Addison’s disease

A
  • autoimmue process
  • tuberculosis (TB)
  • inflammatory process
  • primary neoplasm
  • fungal infection (histoplasmosis)
  • adrenal hemorrhage (anticoagulation therapy)
  • bilateral mets
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4
Q
  • results in..
    • oversecreation of sex hormones and adrenal androgens (hirsutism)
    • congenital causes (impaired synthesis of cortical and aldostrone)
    • acquired causes (tumors)
  • adrenals are symmetrically enlarged
A

adrenogenital syndromes

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5
Q

-hyperaldosteronism
most commonly due to cortical adenoma
-adenomas are more common with females and tend to be small, less than 2cm
- hyperplasia is more common in males
-adrenal carcinoma is a less frequent cause

A

Conn’s Syndrome

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6
Q

clinical symptoms of Conn’s syndrome

A

muscle weakness, hypertension, and abnormal electrocardiogram

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7
Q
  • hypercortisolism
  • causes … adrenal hyperplasia, cortical adenoma, adrenal carcinoma, increase in ACTH-produced by pituitary gland(resulting from pituitary adenoma)
A

Cushing syndrome

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8
Q

-truncal obesity, pencil thin extremities, “buffalo hump”, “moon face”, hypertension, renal stones, irregular menses and psychiatric disturbances

A

Cushing syndrome

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9
Q

results from bilateral hemorrhage into the adrenal glands and caused by severe meningococcal infection

A

Waterhouse-Friderinchsen syndrome

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10
Q

-uncommon, usually small and asymptomatic, females affected more than males, usually unilateral found incidentally, may become calcified

A

adrenal cysts**

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11
Q
  • in adult is usually caused by severe trauma or infection
  • most common in the neonate, caused by the large size of the adrenals and high degree of vascularity
  • sonographically varies depending upon the age of the hemorrhage
A

Adrenal hemorrhage

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12
Q
  • can account for hypersecretion of cortical hormones
  • may be hyperfunctioning or non hyperfunctioning
  • may cause cushing’s syndrome, Conn’s syndrome, or adrenogenital syndrome
  • solid, well-defined, and round
A

Adrenal Adenomas

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13
Q

-rare, highly malignant tumors with poor prognosis
may be hyperfunctional or nonfunctional
-difficult to differentiate from benign adenoma
larger, 3-6cm
-typically well-defined homogenous mass when small
-larger tends to have necrosis, hemorrhage or calcifications
-(rt) tumor may invade IVC and renal veins

A

Adrenal Malignant Tumors

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14
Q
  • commonly caused by primary lung, breast, stomach, colon, or kidney
  • metastases to the adrenal gland typically cause adrenal insufficency
  • differentiation of common benign adenoma is sometimes difficult when there is no other evidence of mets and the adreanl mass is unilateral
A

Adrenal Mets

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15
Q
  • orginate in the adrenal medulla
    • secretes epinephrine and norepinephrine in excessive amounts
    • these hormones produce hypertension
    • associated with severe headaches, tachycardia and palpitations, and excess perspiration
A

Pheochromocytoma

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16
Q

associated with multiple endocrine neoplasm (MEN) and Von Hippel-Lindau disease

A

Pheochromocytoma

17
Q
  • majority are benign
  • usually unilateral, large bulky tumors with a variety of sonographic patterns
  • ectopic adrenal pheochromocytomas are rare but may occur anywhere along the sympathetic nerve chain located parallel to the aorta
A

Phenochromocytoma

18
Q
  • highly malignant tumors of the medulla
  • most common tumor of infancy**
  • most common malignancy of the adrenal glands in childhood**
  • presents as an abdominal mass in childhood
  • typically seen as an echogenic mass with poorly defined margins
  • must be differentiated from Wilm’s tumor (nephroblastoma), and hepatobalstoma
A

Neuroblastoma

19
Q
  • benign, nonfunctioning mas that contains both fat and bone marrow elements
  • hyperechoic mass most commonly seen in the adrenal bed
A

retroperitoneal fat myelipoma

20
Q
  • originates independently within the retroperitoneum
  • most are malignant**
  • types: lyphoma, leiomyoscarcoma, fibrosarcomas and rhabdomyosarcomas
A

primary retroperitoneal tumors

21
Q

-most common primary retroperitoneal tumor

22
Q
  • complex sonographic pattern

- liposarcomas- highly reflective due to fat

A

leiomyosarcoma

23
Q

-may mimic lymphomas and extends across midline

A

fibrosarcomas and rhabdomyosarcomas

24
Q

-refers to enlargement of lymph nodes

A

lymphadenopathy

25
neoplastic conditions assoc. with lymphadenopathy include
- lymphoma - leukemia - metastic disease
26
one of the most common causes of lymphadenopathy
lymphoma, Hodgkin's and non Hodgkin's (much more massive, mesentery involvement more common)
27
- may be seen as anechoic or hypoechoic masses in the para-aortic and paracaval regions - appear sonolucent or hypoechoic because they are homogenous and have no significant interfaces
retroperitoneal lymphadenopathy
28
enlarged nodes anterior and posterior to the mesenteric vessels represent the "sandwich sign"
retroperitoneal lymphadenopthay
29
-enlarged lymph nodes surround mesenteric vessel(s)
sandwich sign
30
- benign or malignant and the retroperitoneal space is the 4th most frequent site - ovaries testes, anterior mediastinum, retroperitoneum and sacrococcygeal region - teratomatous tumors may arise within the upper retroperitoneum and the pelvis
Germ Cell tumors
31
- may contain calcified echoes from bones, cartilage, teeth, and soft tissue elements - teratomas are more common in childhood and are usually located in the upper pole of the left kidney (hetrogeneous and complex)
germ cell tumors
32
- recurrent from previous resected tumors - ex- renal cell CA - ascites, retroperitoneal tumor - liver should be evaluated for metastic involvement and para-aortic region for extension to the lymph nodes
secondary tumors
33
retroperitoneal fluid collections
- urinoma - hemorrhage - abscess
34
-a walled-off collection of extravasated urine that develops spontaneously after trauma, surgery, or a subacute or chronic urinary obstruction
urinoma
35
-may occur in a variety of conditions, including trauma, vasculitis, bleeding, diathesis, leaking aortic aneurysm, or a bleeding neoplasm
hemorrhage
36
-may result from surgery trauma, or perforations of the bowel or duodenum
abscess
37
- a disease of unknown cause and may be associated with malignant process - characterized by thick sheets of fiberous tissue in the retroperitoneal cavity - hyopechoic midline mass**
retroperitoneal fibrosis Ormond's disease