Literature DB >> 26401116

Vaginal angiomatosis: differential diagnosis of a rare case.

Flavio Grauso1, Giancarlo Balbi1, Maria Luisa D'Aponte2, Andrea Ronchi3, Roberto Russo3, Francesca Falcone1, Enrico Michelino Messalli1.   

Abstract

Vaginal angiomatosis is regarded as part of a very rare entity of benign vascular tumors of the female genital tract. The incidence of these tumors is extremely low. The rarity of this disease and lack of distinctive features poses a problem of differential diagnosis. We present the case of a 51-year-old female with grade III uterine prolapse and a bleeding vaginal wall mass. Violaceous irregular soft tissue with hemorrhagic spots was observed in the lower third of the posterior vaginal wall. The patient underwent surgery for colpohysterectomy with vaginal wall mass excision. Surgical excision was curative, and no recurrences were observed after 12 months of follow-up. The aim of our study is to present a rare but representative case. This will hopefully increase the level of awareness regarding this condition so that physicans will keep it in mind during differential diagnosis of similar clinical cases. Furthermore, it highlights the important role of pathological examination for the definitive diagnosis of angiomatosis.

Entities:  

Keywords:  Angiomatosis; hemangioma tumor; vagina

Year:  2015        PMID: 26401116      PMCID: PMC4560480          DOI: 10.5152/jtgga.2015.15018

Source DB:  PubMed          Journal:  J Turk Ger Gynecol Assoc        ISSN: 1309-0380


  9 in total

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8.  HIF-1α and VEGF expression correlates with thrombus remodeling in cases of intravascular papillary endothelial hyperplasia.

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  9 in total
  1 in total

1.  Angiomatosis of the uterus, cervix and fallopian tubes: a rare and benign cause of intractable, heavy menstrual bleeding.

Authors:  Jennifer C Pontré; Victor Ojedo; Bernadette McElhinney
Journal:  BMJ Case Rep       Date:  2017-12-02
  1 in total

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