| Literature DB >> 26699941 |
Ai Miyoshi1, Takashi Miyatake2, Takeya Hara2, Shinnosuke Komiya2, Naoko Komura2, Asuka Tanaka2, Serika Kanao2, Masumi Takeda2, Mayuko Mimura2, Masaaki Nagamatsu2, Masaru Yamasaki2, Takeshi Yokoi2.
Abstract
Malignant primary tumors arising in the uterine broad ligament are extremely rare, and only 26 cases have been reported to date. We describe 2 new cases of primary adenocarcinoma of the broad ligament, and we review the previous literature on such rare tumors. In Case 1, a 71-year-old woman presented with a 2-month history of increased yellow vaginal discharge and lower abdominal pain during bowel movement. Transvaginal sonography revealed a 6.5 cm mass located on the dorsum of the uterus and a 7.0 cm mass (with cystic and solid parts) near the right adnexa. We postoperatively diagnosed the mass as a high-grade serous carcinoma of the broad ligament (pT3cNXM0). The patient is currently receiving adjuvant chemotherapy with paclitaxel and carboplatin. In Case 2, during a complete medical checkup a 43-year-old woman was found to have a pelvic mass indicative of leiomyoma. Transvaginal sonography revealed a 3.8 cm mass located on the dorsum of the uterus. Following surgery, we diagnosed the mass as a clear cell adenocarcinoma of the broad ligament (pT2bN1M0). This patient is also now receiving adjuvant chemotherapy with paclitaxel and carboplatin.Entities:
Keywords: broad ligament; clear cell adenocarcinoma; primary tumor
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Year: 2015 PMID: 26699941 DOI: 10.1177/1066896915622690
Source DB: PubMed Journal: Int J Surg Pathol ISSN: 1066-8969 Impact factor: 1.271