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- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2014
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/18435
Title: | Immunohistochemistry profile of the mucinous lesions of appendiceal and ovarian origin |
Authors: | Vozian, Marin Chemencedji, Inga Negru, Anastasia |
Keywords: | Mucinous lesions;pseudomyxoma peritonei;immunohistochemistry |
Issue Date: | 2014 |
Publisher: | Ministry of Health of the Republic of Moldova, State Medical and Pharmaceutical University Nicolae Testemitanu, Medical Students and Residents Association |
Citation: | VOZIAN, Marin, CHEMENCEDJI, Inga, NEGRU, Anastasia. Immunohistochemistry profile of the mucinous lesions of appendiceal and ovarian origin. In: MedEspera: the 5th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2014, pp. 171-172. |
Abstract: | Introduction: Pseudomyxoma peritonei (PMP) is a rare clinical entity, characterized by a
significant amount of mucinous ascites associated by peritoneal mucinous implants. The most frequent
localization of primary lesion are the appendix and ovaries (epithelial mucinous lesions with varying histopathological architecture), although other primary sites of origin were described: gallbladder,
stomach, pancreas, colon, uterus, fallopian tubes, urinary bladder, breast and lungs. There are still
ongoing discussions in the literature about PMP, especially regarding the origins, histopathology and
adequate treatment. The biological potential of the lesions depends on several factors which may be
determined at the morphological examination. The primary aim is to identify the primary lesion site. In
majority of PMP cases the primary lesion is originating from appendix. In some cases, though, there
may be metastases to the ovaries, which need to be differentiated from primary mucinous ovarian
lesions, especially in condition of grossly normal appendix. Taking in consideration all mentioned
above, epithelium from different sites manifest different immunohistochemical expressions and this
may help to identify the primary lesion site. Ovary epithelium and majority of tumors originating from
the ovary manifest positive expression for cytokeratin 7 (CK 7) and are negative for cytokeratin 20 (CK
20), while appendiceal epithelium and tumors originating from appendix and colon are positive for CK
20 and negative for CK 7. Another specific immunohistochemical marker for colorectal and appendiceal
origin tumors is the carcinoembrionic antigen (CEA).
Materials and methods: Current paper included two cases of ovarian mucinous
cystadenoma, two cases of PMP of appendiceal origin (mucinous cystadenocarcinom a) and one
case of appendiceal mucinous cystadenocarcinoma.
An immunohistochemical profile including CK 7, CK 20 and CEA for all the specimens was perfonned.
Results: For cases of PMP of appendiceal origin (n=2) and appendiceal mucinous
cystadenocarcinoma (n=l) a positive expression of CK 20 and CEA was obtained, manifested by
moderate and/or intense reaction in cytoplasm and membrane of majority of tumor cells (C++/+++;
M++/+++). Reaction for CK 7 was negative.
For cases of ovarian mucinous cystadenoma (n=2) a positive expression of CK 7 was
obtained, manifested by intense reaction in cytoplasm and membrane of the tall prismatic
epithelium (C+++; M+++). Reaction for CK 20 and CEA was negative.
Conclusion: Results obtained within the current study showed a difference of the
immunohistochemical profile of the mucinous lesions of appendiceal and ovarian origin, thus
confirming the available data. These findings prove that the immunohistochemical profiling may
help to identify the origin of the primary lesion and this have an impact on the subsequent
management of these patients. |
metadata.dc.relation.ispartof: | MedEspera: The 5th International Medical Congress for Students and Young Doctors, May 14-17, 2014, Chisinau, Republic of Moldova |
URI: | http://repository.usmf.md/handle/20.500.12710/18435 |
Appears in Collections: | MedEspera 2014
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