2015
DOI: 10.3126/kumj.v11i3.12515
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Fallopian Tube Papilloma – Case Report of a Rare Tumor

Abstract: Fallopian tube neoplasms are rare. We report a rare case of fallopian tube papilloma discovered incidentally in a 45 year old female, operated for procidentia. Right tube was dilated at the infundibular region, with friable grey white tissue in the lumen. Microscopy showed delicate branching papillae lined by a single layer of epithelium resembling tubal lining. There were no features to suggest a reactive hyperplasia in response to inflammation or of aggressive behaviour. KEY WORDSEpithelial lesions, fallopia… Show more

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Cited by 3 publications
(4 citation statements)
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“…FT papillomas are rare tumors of the tube, with only eight cases reported so far in English literature, ours being the ninth such case [1,3,4]. These tumors are either discovered incidentally [1] or they may be symptomatic presenting as a mass lesion [3]. In our case, the tumor was incidentally found in a patient who was clinically and sonologically diagnosed as tubal gestation, which might have occurred secondary to tubal obstruction caused by papilloma.…”
Section: Discussionmentioning
confidence: 57%
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“…FT papillomas are rare tumors of the tube, with only eight cases reported so far in English literature, ours being the ninth such case [1,3,4]. These tumors are either discovered incidentally [1] or they may be symptomatic presenting as a mass lesion [3]. In our case, the tumor was incidentally found in a patient who was clinically and sonologically diagnosed as tubal gestation, which might have occurred secondary to tubal obstruction caused by papilloma.…”
Section: Discussionmentioning
confidence: 57%
“…Benign tumors of the tube include polypoid adenofibromas, papilloma, metaplastic papillary tumor and benign serous cystadenoma [2]. FT papillomas are rare tumors of the tube, with only eight cases reported so far in English literature, ours being the ninth such case [1,3,4]. These tumors are either discovered incidentally [1] or they may be symptomatic presenting as a mass lesion [3].…”
Section: Discussionmentioning
confidence: 93%
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“…The Cotyledonoid dissecting leiomyoma (CDL), also called sternberg tumor, is a rare subtype of leiomyoma that typically manifests in the uterus [1]. Macroscopically, the tumors exhibit multiple nodules, a dark red hue, and a placental-like appearance.…”
Section: Introductionmentioning
confidence: 99%