Renal 2 Flashcards

1
Q

Autosomal dominant

A

Adults

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2
Q

Autosomal recessive

A

Pediatric

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3
Q

The most common renal cyst

A

Simple cyst

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4
Q

Typical in patients with renal replacement therapy

A

Acquired cystic kidney disease

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5
Q

Associated with increased risk of renal tumors

A

Acquired cystic kidney disease

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6
Q

Lined by simple cuboidal or flat cells

A

Acquired cystic kidney disease

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7
Q

The extra renal manifestations of the autosomal dominant PKD

A
  • Polycystic liver disease.
  • Mitral valve prolapse.
  • Berry aneurysm.
  • SAH.
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8
Q

Mutations of PKD1 chr. 16 and PKD2 ch. 4 are associated with

A

ADPKD

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9
Q

Mutation of PKHD1 ch. 6 is associated with

A

Autosomal recessive PKD

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10
Q

Polycystin proteins are associated with

A

ADPKD

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11
Q

fibrocystin proteins are associated with

A

ARPKD

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12
Q

Regulates differentiation of renal collecting duct and biliary epithelium

A

Fibrocystin

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13
Q

Sponge like appearance in cut surface of the kidney is a feature of?

A

ARPKD

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14
Q

The commonest renal tumor

A

Renal cell carcinoma

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15
Q

The most common predisposing factor of renal cell tumors

A

Smoking in 50% (then obesity 25%)

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16
Q

The classic clinical triad that is seen in only 10% of RCC patients

A

Flank pain - palpable mass - painless hematuria

17
Q

25% of patients with RCC have radiological evidence of metastasis from

A

Lung (>50%)

Bones (33%)

18
Q

Hom tan brown solitary spherical

A

Chromophobe RCC

19
Q

VHL gene mutation is associated with?

  • CCRCC.
  • Papillary RCC.
  • Chromophobe RCC.
  • Unclassified.
A

A

20
Q

Loss of VHL gene leads to ……. HIF-1 which stimulates unchecked cell growth and angiogenesis.

A

Increased HIF-1 ( hypoxia induced factor 1)

21
Q

Hs bright yellow (lipid) usually with areas of grey white necrosis and foci of hemorrhagic discoloration

A

Clear cell RCC

22
Q

< 7 cm tumor which is NOT invading the Gerota’s fascia is class …….. CCRCC

A
Stage 1
( >7 cm= 2, extends to the major veins but not beyond the Gerota’s fascia= 3, beyond it= 4)
23
Q

Have abundant clear to granular eosinophilic cytoplasm (contains glycogen and lipids)

A

CCRCC

24
Q

Have VHL gene mutation, same as CCRCC

A

Multilocular cystic CCRCC

25
Q

Cysts are lined by clear cells with low grade nuclei are seen in?

A

Multilocular cystic CCRCC

26
Q

The 2nd most common type of RCC

A

Papillary RCC

27
Q

Which one have better prognosis CCRCC or PRCC?

A

PRCC

28
Q

Finger like projections of fibrovascular stroma lined by neoplastic epithelial cells + foamy histiocytes + psammoma bodies are seen in?

A

PRCC

29
Q

Have excellent prognosis compared to CC and papillary RCC

A

Chromophobe

30
Q

Abundant finely reticulated pale cytoplasm + thick cell membrane are seen in

A

Chromophobe RCC

31
Q

Perinuclear halo + large koilocytic nuclei (wrinkled nuclear membrane)

A

Chromophobic RCC

32
Q

Over-expression of TFE3 protein is associated with

A

MiT family translocation RCC

33
Q

Large irregular and eccentric nuclei and prominent nucleoli + central eosinophilic intracytoplasmic inclusions

A

Rhabdoid differentiation

34
Q

Solid nests + Stroma often edematous hypocellular particularly in central scar + No papillae, necrosis, frequent mitoses or clear cells.

A

Oncocytoma

35
Q

Urothelial carcinoma can be diagnosed by

A

Urine cytology

36
Q

Exposure to amino dyes and schistozoma hematobium is associated with

A

Urothelial carcinoma

37
Q

The commonest pediatric renal tumor

A

Nephroblastoma (Wilm’s tumor)

38
Q

Associated with tuberous sclerosis

A

Angiomyolipoma

39
Q

Cartwheel arrangement is seen in

A

Angiomyolipoma