Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/24936
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dc.contributor.authorBasheska, Nelien_US
dc.contributor.authorKrstevska, Iskraen_US
dc.contributor.authorOgnenoska-Jankovska, Biljanaen_US
dc.date.accessioned2022-12-15T13:09:02Z-
dc.date.available2022-12-15T13:09:02Z-
dc.date.issued2018-10-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/24936-
dc.descriptionCongress Booklet - Abstracts of Posters and Oral Presentations, pp49en_US
dc.description.abstractObjective: Granular cell tumors (GCTs) are relatively uncommon soft tissue tumors that are usually benign (0.5-2.0% malignant). They have been described in many sites and organs, although cases with genital involvement have rarely been reported. We present the clinicopathological features of a case of a uterine corpus GST. Methods: A 37-year-old woman with secondary infertility was admitted at the University Clinic of Gynecology and Obstetrics for a hysteroscopic examination during which a polypoid isthmico-cervical lesion was detected. Results: The biopsy excision specimen consisted of one smaller fragment of the endometrium and two larger semispherical fragments measuring 0.7x0.5x0.4 and 0.8x0.6x0.4 cm. Upon microscopic examination of the larger fragments under the partly pseudodecidualized endometrial or isthmic type of surface mucosa, a benign mesenchymal neoplasm was found composed of nests of large polygonal cells with an abundant eosinophilic granular cytoplasm and round to oval nuclei lacking conspicuous nucleoli or mitotic figures. In addition to PAS positivity, upon immunohistochemical staining, the large cells also showed vimentin, S-100, neuron-specific enolase, CD56, CD57, calretinin and Wilms tumor 1 positivity. The proliferative index determined by Ki-67 staining was <5%. Based on the pathological and immunohistochemical examinations, the diagnosis of a benign GCT was established. Due to the fact that the neoplasm was incompletely excised a wide local excision was recommended along with a careful follow-up of the patient. The patient refused the excision and is being well and preparing for in vitro fertilization 24 months following biopsy. Conclusion: GCTs of the uterus and especially of the uterine corpus are extremely rare. To the best of our knowledge, this is a second reported case of uterine corpus GCT in the English-language literature. It is important for gynecologists as well as pathologists to be aware of the possibility of uterine corpus GCTs, for which accurate diagnosis, complete resection and long-term follow-up are crucial.en_US
dc.language.isoenen_US
dc.publisherThe Arab Division of the International Academy of Pathology In Collaboration with the Jordanian Society of Pathologistsen_US
dc.subjectgranular cell tumoren_US
dc.subjectuterine corpusen_US
dc.subjecthistologyen_US
dc.subjecthistochemistryen_US
dc.subjectimmunohistochemistryen_US
dc.titleBenign granular cell tumor of the uterine corpus: A case reporten_US
dc.typeProceeding articleen_US
dc.relation.conferenceThe XXXII Congress of the International Academy of Pathology & 30th Congress of the Arab Division of IAP, 14-18 October, 2018, Dead Sea, Jordan.en_US
item.fulltextWith Fulltext-
item.grantfulltextopen-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Conference papers
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