Difference between revisions of "Peutz-Jeghers syndrome"

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(fix ref)
(→‎Clinical: +SCTAT)
Line 5: Line 5:
*Melanocytic macules.  
*Melanocytic macules.  
**Lips, buccal mucosa, and digits.  
**Lips, buccal mucosa, and digits.  
**Multiple [[Peutz-Jeghers polyps]].
*Multiple [[Peutz-Jeghers polyps]].


Increased risk of various neoplasms - primarily:
Increased risk of various neoplasms - primarily:
Line 12: Line 12:
**[[Granulosa cell tumour]].
**[[Granulosa cell tumour]].
**[[Sertoli cell tumour]] - esp. with calcification.
**[[Sertoli cell tumour]] - esp. with calcification.
Reported associations:
*Associated with (ovarian) SCTAT (sex cord tumour with annular tubules).<ref name=pmid7358344>{{cite journal |author=Purohit RC, Alam SZ |title=Sex cord tumour of the ovary with annular tubules (SCTAT) |journal=Histopathology |volume=4 |issue=2 |pages=147–54 |year=1980 |month=March |pmid=7358344 |doi= |url=}}</ref>


==Microscopic==
==Microscopic==

Revision as of 12:51, 26 April 2011

Peutz-Jeghers syndrome is a constellation of findings inherited with an autosomal dominant pattern due to a defect in the STK11 gene.

Clinical

Features:[1]

Increased risk of various neoplasms - primarily:

Reported associations:

  • Associated with (ovarian) SCTAT (sex cord tumour with annular tubules).[4]

Microscopic

Features:[5][6]

  • Frond-like polyp with all three components of mucosa:
    1. Muscosal epithelium (melanotic mucosa, goblet cells).
    2. Lamina propria.
    3. M. mucosae.

Image:

See also

References

  1. URL: http://www.ncbi.nlm.nih.gov/omim/175200. Accessed on: 13 July 2010.
  2. Beggs AD, Latchford AR, Vasen HF, et al. (July 2010). "Peutz-Jeghers syndrome: a systematic review and recommendations for management". Gut 59 (7): 975–86. doi:10.1136/gut.2009.198499. PMID 20581245.
  3. URL: http://www.ncbi.nlm.nih.gov/omim/175200. Accessed on: 22 December 2010.
  4. Purohit RC, Alam SZ (March 1980). "Sex cord tumour of the ovary with annular tubules (SCTAT)". Histopathology 4 (2): 147–54. PMID 7358344.
  5. Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease (7th ed.). St. Louis, Mo: Elsevier Saunders. pp. 859. ISBN 0-7216-0187-1.
  6. Bronner, MP. (Apr 2003). "Gastrointestinal inherited polyposis syndromes.". Mod Pathol 16 (4): 359-65. doi:10.1097/01.MP.0000062992.54036.E4. PMID 12692201. http://www.nature.com/modpathol/journal/v16/n4/full/3880773a.html.