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伴有大量淋巴细胞浸润的子宫肌瘤——病例报告

Uterine myoma with massive lymphocytic infiltration - case report.

作者信息

Wasyluk Tomasz, Obrzut Bogdan, Gałązka Krystyna, Żmuda Marcin, Obrzut Marzanna, Darmochwał-Kolarz Dorota

机构信息

Department of Obstetrics and Gynaecology, Provincial Clinical Hospital No. 2 in Rzeszow, Poland.

Department of Pathomorphology, Jagiellonian University Medical College, Krakow, Poland.

出版信息

Prz Menopauzalny. 2019 Jun;18(2):123-125. doi: 10.5114/pm.2019.86838. Epub 2019 Jun 28.

Abstract

INTRODUCTION

Uterine leiomyomas are the most common neoplasm of the uterus in women. Massive lymphocytic infiltration in a myoma is an unusual finding. It is characterised by the varying intensity of lymphocyte infiltration, the presence of scattered plasma cells, eosinophilia, and rarely, other items. We would like to call attention to such a rare lesion.

CASE DESCRIPTION

We present the case of a 31-year-old woman who had undergone surgical excision of a uterine tumour. Grossly, it had the typical uterine smooth muscle wall consistency. The microscopic examination revealed leiomyoma with heavy infiltration composed mainly of lymphocytes. On immunohistochemistry, in the lymphocytic infiltrate the T mature (CD3+/CD5+/TdT-) lymphocytes, small and of cytotoxic (CD8+/CD56-) type, prevailed, with moderate proliferative activity (expression of Ki67 found in ca. 30-40% of the cells), whereas B lymphocytes (CD20+/CD5-/TdT-) were innumerous and present in nodular aggregates. Despite a strong suspicion of neoplastic lymphoproliferation, the histopathological diagnosis was: leiomyoma with massive lymphoid infiltration. The cause of this feature is not known, although the gonadotropin-releasing hormone agonist and post-menopausal processes may promote such transformations. In differential diagnosis, malignant lymphoma, inflammatory pseudotumour, and pyomyoma should be included.

CONCLUSIONS

Lymphocytic infiltration within the uterine myoma is rare. The recognition of its distinct histological features is important to avoid possible misdiagnosis.

摘要

引言

子宫平滑肌瘤是女性子宫中最常见的肿瘤。肌瘤中出现大量淋巴细胞浸润是一种不寻常的发现。其特征为淋巴细胞浸润强度各异,存在散在的浆细胞、嗜酸性粒细胞,且很少有其他成分。我们希望引起对这种罕见病变的关注。

病例描述

我们报告一例31岁女性,她接受了子宫肿瘤的手术切除。大体上,其具有典型的子宫平滑肌壁质地。显微镜检查显示为平滑肌瘤伴大量主要由淋巴细胞组成的浸润。免疫组织化学检查显示,在淋巴细胞浸润中,以成熟的T淋巴细胞(CD3+/CD5+/TdT-)为主,呈小的细胞毒性(CD8+/CD56-)型,具有中等增殖活性(约30 - 40%的细胞表达Ki67),而B淋巴细胞(CD20+/CD5-/TdT-)数量较少,呈结节状聚集。尽管强烈怀疑为肿瘤性淋巴细胞增殖,但组织病理学诊断为:平滑肌瘤伴大量淋巴细胞浸润。虽然促性腺激素释放激素激动剂和绝经后过程可能促进这种转变,但其原因尚不清楚。在鉴别诊断中,应包括恶性淋巴瘤、炎性假瘤和脓性肌瘤。

结论

子宫肌瘤内的淋巴细胞浸润罕见。认识其独特的组织学特征对于避免可能的误诊很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e28/6719633/3c2fdec7764f/MR-18-86838-g001.jpg

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