Difference between revisions of "Juvenile granulosa cell tumour"

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{{ Infobox diagnosis
| Name      = {{PAGENAME}}
| Image      = Juvenile_granulosa_cell_tumour_-_very_high_mag.jpg
| Width      =
| Caption    = Juvenile granulosa cell tumour. [[H&E stain]].
| Synonyms  =
| Micro      = microcystic spaces, cuboidal-to-polygonal cells in sheets or stands or cords, with moderate-to-marked nuclear atypia, and basophilic cytoplasm
| Subtypes  =
| LMDDx      = [[Brenner tumour]]
| Stains    =
| IHC        = inhibin +ve, calretinin +ve
| EM        =
| Molecular  =
| IF        =
| Gross      = mass lesion, solid
| Grossing  =
| Site      = [[ovary]] - ''[[ovarian tumours]]''
| Assdx      =  [[endometrial hyperplasia]], [[endometrioid endometrial carcinoma]]
| Syndromes  =
| Clinicalhx =
| Signs      =
| Symptoms  = +/-menorrhagia
| Prevalence = uncommon
| Bloodwork  =
| Rads      =
| Endoscopy  =
| Prognosis  =
| Other      =
| ClinDDx    =
| Tx        =
}}
'''Juvenile granulosa cell tumour''' is an uncommon [[ovarian tumour]] in the ''sex cord stromal tumours'' group.
'''Juvenile granulosa cell tumour''' is an uncommon [[ovarian tumour]] in the ''sex cord stromal tumours'' group.


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**May present as precocious puberty.<ref name=pmid21526089>{{Cite journal  | last1 = Hashemipour | first1 = M. | last2 = Moaddab | first2 = MH. | last3 = Nazem | first3 = M. | last4 = Mahzouni | first4 = P. | last5 = Salek | first5 = M. | title = Granulosa cell tumor in a six-year-old girl presented as precocious puberty. | journal = J Res Med Sci | volume = 15 | issue = 4 | pages = 240-2 | month = Jul | year = 2010 | doi =  | PMID = 21526089 }}</ref>
**May present as precocious puberty.<ref name=pmid21526089>{{Cite journal  | last1 = Hashemipour | first1 = M. | last2 = Moaddab | first2 = MH. | last3 = Nazem | first3 = M. | last4 = Mahzouni | first4 = P. | last5 = Salek | first5 = M. | title = Granulosa cell tumor in a six-year-old girl presented as precocious puberty. | journal = J Res Med Sci | volume = 15 | issue = 4 | pages = 240-2 | month = Jul | year = 2010 | doi =  | PMID = 21526089 }}</ref>
*Reported in males.<ref>URL: [http://path.upmc.edu/cases/case631.html http://path.upmc.edu/cases/case631.html]. Accessed on: 26 January 2012.</ref>
*Reported in males.<ref>URL: [http://path.upmc.edu/cases/case631.html http://path.upmc.edu/cases/case631.html]. Accessed on: 26 January 2012.</ref>
*Uncommon.<ref name=pmid23033282>{{Cite journal  | last1 = Oztekin | first1 = D. | last2 = Kurt | first2 = S. | last3 = Camuzcuoglu | first3 = H. | last4 = Balsak | first4 = D. | last5 = Dicle | first5 = N. | last6 = Tinar | first6 = S. | title = Granulosa cell tumors of the ovary: review of 43 cases. | journal = J BUON | volume = 17 | issue = 3 | pages = 461-4 | month =  | year =  | doi =  | PMID = 23033282 }}</ref>


==Gross==
==Gross==
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Notes:
Notes:
*Juvenile variant of GCT has more nuclear pleomorphism.
*Juvenile variant of GCT has more nuclear pleomorphism.
DDx:
*[[Brenner tumour]].


===Images===
===Images===
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