Pathology Flashcards

(64 cards)

1
Q

Primary causes of Nephrotic syndrome

A

Minimal change
Focal segmented Glomerular sclerosis
membranous
Membranoproliferative

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2
Q

inflammation of the glans penis. Associated with poor hygiene - rare in circumcised individuals.

A

Balanitis

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3
Q

primary stage chancre heals within to weeks caused by treponemma pallidum

A

syphilis

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4
Q

morphology of N. gonorrhea

A

intracellular gram negative diplococci

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5
Q

the N. gono cause

A

acute purulent urethritis associated with prostatitis and epididymitis

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6
Q

Ch. trachomatis cause

A

non- gonococcal urethritis

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7
Q

Related to the accumulation of squamous cell & inflammatory debris

A

Carcinoma in situ

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8
Q

Infection with high-risk HPV

A

Carcinoma in situ
squamous cell carcinoma

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9
Q

Developmental failure of a testis to descend into the scrotum.

A

cryptorchidism

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10
Q

continuity of the tunica vaginalis with the peritoneal cavity

A

Hydrocele

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11
Q

Hydroceles can be distinguishedvclinically from solid testicular tumorsv by

A

physical examination and
transillumination.

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12
Q

blood accumulation of blood distending the
tunica vaginalis. Most often caused by trauma, or
occasionally due to a tumor.

A

Hematocele

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13
Q

varicose dilation of multiple veins of the
spermatic cord

A

Varicocele

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14
Q

sperm-containing cyst. Most often intratesticular.

A

Spermatocele

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15
Q

testicular atrophy

A

often unknown etiology
orchitis
trauma
disorder of hypothalamus or pitutary
hormonal therapy as estrogen
liver cirrhosis
cryptorchidism
klinefelter syndrome
chronic deblititating disease
old age

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16
Q

cause of bacterial orchitis

A

syphilis associated with epididymitis

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17
Q

cause of viral orchitis

A

mumps

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18
Q

causes of epididymitis

A

N. Gono
C. trachomatis
E.coli
M. tuberculosis

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19
Q

the most common testicular germ cell tumor

A

seminoma

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20
Q

Analogous to ovarian dysgerminoma

A

Seminoma

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21
Q

associated with increased serum hCG

A

Seminoma
Embryonal carcinoma
choriocarcinoma

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22
Q

give metastases to abdominal lymph nodes

A

Seminoma

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23
Q

Comprised of three distinct cell types, lacks ITGCN with no significant lymphocytic response

A

spermatocytic seminoma

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24
Q

large cells withcentrally located nuclei and
prominent nucleoli. Fibrous septa separate nests of tumor cells

A

Seminoma

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25
compare between spermatocytic and conventional seminoma
spermatocytic: no ITGCN no lymphocytic response conventional: have ITGCN and lymphocytic inflitrate
26
Analogous to similar ovarian tumor
Embryonal carcinoma
27
Increase in serum AFP (alpha fetoprotein)
Endodermal sinus (yolk sac) tumor
28
most common testicular tumor in infacy and early childhood
Endodermal sinus (yolk sac) tumor
29
morphologicaly has Schiller-Duval body
Endodermal sinus (yolk sac) tumor
30
Germ cell tumor is derived from two or more embryonic layers
teratoma
31
involve Multiple tissue types: such as cartilage islands, ciliated epithelium, liver cells, neuroglia, embryonic gut, or striated muscle.
Teratoma
32
the three types of teratoma
mature: always malignant immature: behavior is malignant teratoma with malignant transformation: contains malignant tissue, such as squamous cell carcinoma
33
highly chemosensitive
Choriocarcinoma
34
Characterized by intracytoplasmic Reinke crystals
Leydig cell tumor
35
Androgen-producing
Leydig cell tumor
36
Testicular Sex Cord Stromal tumors
Leydig cell tumor sertoli cell tumor Granulosa cell tumor
37
Associated with precocious puberty in children and gynecomastia in adults
Leydig cell tumor
38
related to the action of dihydrotestosterone (DHT)
Benign Prostatic Hyperplasia
39
promote expression of receptors for DHT
estrogen
40
DHT is synthesized from
testosterone
41
DHT is synthesized from testosterone by the action of
5α-reductase, type 2
42
Inhibition of which enzyme is one approach to the treatment of BPH
5 alpha reductase
43
Early stage of adenocarcinoma
increased PSA
44
late stage of adenocarcinoma
increased serum prostatic acid phosphatase
45
Bony osteoblastic metastasis from adenocarcinoma
increased serum alkaline phosphatase
46
effacement of glomerular foot processes without antibody deposits.
minimal change disease
47
Most frequent cause of nephrotic syndrome in children
minimal change disease (nephrotic)
48
Glomeruli show focal and segmental obliteration of capillary lumina
Focal segmental glomerulosclerosis
49
nonspecific trapping of IgM and C3
Focal segmental glomerulosclerosis
50
Most often directed against the PLA2R on podocytes
Membranous nephropathy
51
LM: diffuse capillary wall thickening. IF: Granular subepithelial deposits of antibodies IgG and C3
Membranous nephropathy
52
Type 1 is an immune complex–mediated disease with immune deposits in the subendothelial location.
Membranoproliferative glomerulonephritis
53
GBM “spike” formation
membranous nephropathy
54
Deposition of immune complexes, mainly in the subepithelial spaces, with abundant neutrophils and proliferation of glomerular cells.
Acute postinfectious glomerulonephritis
55
Primarily subepithelial humps.
Acute postinfectious glomerulonephritis
56
Granular deposits (IgG, IgM and C3 along GBM and mesagium)
Acute postinfectious glomerulonephritis
57
Most common form of glomerulonephritis worldwide
IgA nephropathy
58
Mesangial deposits of IgA containing immune complexes
IgA nephropathy
59
showing subtle mesangial hypercellularity
IgA nephropathy
60
mesangial electrondense deposits.
IgA nephropathy
61
caused by mutations in genes encoding GBM/type IV collagen
Hereditary nephritis (Alport syndrome)
62
Hereditary nephritis (Alport syndrome)
mutations in genes encoding GBM/type IV collagen | It manifests as hematuria and slowly progressing proteinuria
63
benign nonprogressive disorder caused by mutation encoding GBM
thin basement membrane disease
64
Severe glomerular injury with necrosis, GBM breaks, and proliferation of parietal epithelium (crescents)
Rapidly Progressive Glomerulonephritis