Difference between revisions of "Undescended testis"

From Libre Pathology
Jump to navigation Jump to search
 
(2 intermediate revisions by the same user not shown)
Line 11: Line 11:
*Type III cases diffuse tubular hypoplasia.
*Type III cases diffuse tubular hypoplasia.
*Type IV diffuse Sertoli cell hyperplasia.
*Type IV diffuse Sertoli cell hyperplasia.
DDx:
*[[Germ cell neoplasia in situ]].
==Sign out==
<pre>
A. Right Testis, Orchiectomy:
- Benign testis with germ cell hypoplasia, absent Leydig cells and absent spermatogenesis.
- Unremarkable epididymis.
- NEGATIVE for germ cell neoplasia.
Comment:
The findings are compatible with an undescended testis.
</pre>


==See also==
==See also==

Latest revision as of 15:37, 28 May 2026

Undescended testis, also cryptorchidism, is when the testis fails to descend into the scrotum - from it embryological origin in the abdomen.

General

  • Right more common than left.
    • In a larger series: 218 on left side, 459 right side and 96 bilateral.[1]

Microscopic

Four patterns are described by Nistal et al.:[2]

  • Type I cases testes with minimal lesions.
  • Type II cases marked germinal hypoplasia as well as slight or marked tubular hypoplasia.
  • Type III cases diffuse tubular hypoplasia.
  • Type IV diffuse Sertoli cell hyperplasia.

DDx:

Sign out

A. Right Testis, Orchiectomy:
	- Benign testis with germ cell hypoplasia, absent Leydig cells and absent spermatogenesis.
	- Unremarkable epididymis.
	- NEGATIVE for germ cell neoplasia.

Comment:
The findings are compatible with an undescended testis.

See also

References

  1. You J, Li G, Chen H, Wang J, Li S (March 2020). "Laparoscopic orchiopexy of palpable undescended testes_ experience of a single tertiary institution with over 773 cases". BMC Pediatr 20 (1): 124. doi:10.1186/s12887-020-2021-6. PMC 7075009. PMID 32178653. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075009/.
  2. Nistal M, Paniagua R, Díez-Pardo JA (November 1980). "Histologic classification of undescended testes". Hum Pathol 11 (6): 666–74. doi:10.1016/s0046-8177(80)80078-5. PMID 6108912.