[Pseudocarcinomatous hyperplasia of the fallopian tube: a clinicopathological analysis of sixteen cases].

Q3 Medicine
Y H Sun, X C Chen, Y P Xiao, X Tao, W Y Gu
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引用次数: 0

Abstract

Objective: To investigate the clinicopathological features, diagnosis and differential diagnosis of pseudocarcinomatous hyperplasia of the fallopian tubes. Methods: Sixteen cases of pseudocarcinomatous hyperplasia of the fallopian tubes diagnosed at Obstetrics and Gynecology Hospital of Fudan University from January 2011 to January 2024 were collected.The pathological sections were reviewed, the clinical and pathological data were consulted, and immunohistochemical examination was conducted along with follow-up. Results: The patients were aged from 19 to 57 years, with an average age of 41 and a median age of 38. Among the 16 cases, 4 were located in the right fallopian tubes, 6 in the left fallopian tubes, while the remaining cases presented bilaterally. The general manifestations were tubal edema, crispness and purulent secretion in the lumen. Morphologically, the fallopian tube mucosa exhibited a significant infiltration of neutrophils, lymphocytes and plasma cells. The epithelial cells of the fallopian tube displayed evident proliferation, stratification and disorganized arrangement leading to formation of small glandular cavity with back-to-back, fissure-like and sieve-like structures. Immunohistochemical analysis revealed positivity for CK7 and WT1, along with wild-type p53 expression, Ki-67 index ranged from 5% to 20%. During the follow-up period ranging from 1 to 156 months, all the patients remained free of disease. Conclusions: Pseudocarcinomatous hyperplasia of the fallopian tube is a rare non-neoplastic lesion, which can lead to epithelial hyperplasia and atypical hyperplasia. The most important significance of recognizing this lesion lies in avoiding misdiagnosis of fallopian tube cancer during intraoperative and postoperative pathological examination. This ensures that clinicians can administer correct clinical interventions.

[输卵管假癌性增生:十六例临床病理分析]。
目的探讨输卵管假癌性增生的临床病理特征、诊断和鉴别诊断。方法收集2011年1月至2024年1月复旦大学附属妇产科医院确诊的16例输卵管假癌增生病例,回顾病理切片,查阅临床和病理资料,并进行免疫组化检查和随访。结果患者年龄 19 至 57 岁,平均年龄 41 岁,中位年龄 38 岁。16 例病例中,4 例位于右侧输卵管,6 例位于左侧输卵管,其余病例为双侧输卵管。一般表现为输卵管水肿、变脆和管腔内有脓性分泌物。从形态上看,输卵管粘膜有大量中性粒细胞、淋巴细胞和浆细胞浸润。输卵管上皮细胞明显增生、分层和排列紊乱,形成背靠背、裂隙状和筛状结构的小腺腔。免疫组化分析显示,CK7 和 WT1 呈阳性,野生型 p53 也有表达,Ki-67 指数为 5%-20%。在 1 至 156 个月的随访期间,所有患者均未再发病。结论输卵管假癌性增生是一种罕见的非肿瘤性病变,可导致上皮增生和非典型增生。认识这种病变最重要的意义在于避免在术中和术后病理检查中误诊为输卵管癌。这将确保临床医生能够采取正确的临床干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
中华病理学杂志
中华病理学杂志 Medicine-Medicine (all)
CiteScore
1.00
自引率
0.00%
发文量
10377
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