Lubitz Male Hypogonadism Flashcards

1
Q

2 Causes of Hyper-Gonadotropic Hypogonadism

A
  1. Klinefelter

2. Cryptoorrchidism

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2
Q

Within each testis-lobule are two to four loops of seminiferous tubules. Each loop empties into an anastomosing network of tubules called the ______

A

Rete Testis

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3
Q

Among the pituitary dysfunctions causing HYPOgonadotropic hypogonadism, is Hyper-_______ which inhibits GnRH

A

Prolactinemia

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4
Q

Klinefelter’s is a genotype of _____ w/ what levels of T, LH/FSH?

A

XXY male w/ low T and High LH/FSH

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5
Q

Sem Tubule —> Rete Testis –>efferent ductules –> _____

A

Head of epididymis

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6
Q

Sertoli Cells express both _____ Receptor and _____ Receptor

A
  • Androgen

- FSH

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7
Q

XXY males results in small testis, low T, and HIGH LH/FSH in ______ Syndrome

A

Klinefelter’s

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8
Q

Testosterone can be converted into a potent, nonaromatizable androgen, 5α-dihydrotestosterone (DHT), by the enzyme _____. This enzyme has Type 1 and Type 2, with Type 2 having the most notable, widespread effects

A

5α-reductase

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9
Q

Leydig cells’ main function is to produce _____

A

Testosterone

“Dig that T”

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10
Q

Leydig Cells express _____ Receptor

A

LH

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11
Q

Inhibin is made from Sertoli cells and exclusively inhibits the production of _____

A

FSH

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12
Q

Unlike the Zona Reticularis of the Adrenal, the Leydig cell expresses a Leydig cell-specific isoform of 17β-hydroxysteroid dehydrogenase (17βHSD3), which converts _______ to testosterone

A

androstenedione

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13
Q

Without Testosterone, the male parts originating from the ______ duct still form

A

Mesonephric

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14
Q

A small phallus means that the hypogonadism occurred when?

A

Pre-Pubertal

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15
Q

4 Side effects of Testosterone Replacement

A
  1. Dyslipidemia
  2. Polycythemia
  3. Gynecomastia
  4. Growth of Prostate
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16
Q

“Some Hormones Create Knockers” is a mnemonic for drugs that cause gynecomastia

A
  • Spirinolactone
  • Hormones
  • Cimetidine
  • Ketoconazole
17
Q

3 causes of hypo-gonadotropic hypogonadism

A
  1. Kallman
  2. Prader-willi
  3. Pituitary adenoma
18
Q

Kallman syndrome, Parder-Willi Syndrome, and Pituitary adenomas all cause ______ gonadotropic hypogonadism

A

HYPO

19
Q

Pathophys of Kallmann-caused hypogonadotropic hypogonadism

A

GnRH neurons fail to travel along with smell receptors

20
Q

If you have Orchitis due to Mumps or HIV, what happens to T,LH,FSH levels?

A
  • Low T
  • High FSH/LH
    (Pituitary in tact)
21
Q

Key physical finding with Kallmann’s syndrome?

A

Anosmia

22
Q

Klinefelter syndrome, CryptoOrchidism, and trauma/autoimmune are 3 causes of ________ -gonadotropic hypogonadism

A

HYPER

23
Q

Eunuchoidism clues you that the hypogonadism occurred at what time?

A

Pre-Pruberty

24
Q

Four Additional functions of Chef Sertoli Cells

A
  1. CYP19 Aromatase to make estradiol-17B
  2. Androgen-Binding Protein (ABP)
  3. Anti-Mullerian Hormone (AMH)
  4. Inhibin (Just FSH Negative Feedback)
25
Q

Both LH and FSH act via which signaling pathway? (3 parts)

A

Gs-cAMP-PKA

26
Q

Cholesterol is converted to pregnenolone by CYP11A1 (cholesterol desmolase). Pregnenolone is then processed to progesterone, 17α-hydroxyprogesterone, and androstenedione by _____ and _____.

A
  • 3β-hydroxysteroid dehydrogenase type 2 (3β-HSD2)

- 17hydroxylase/17,20-lyase (CYP17)