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本文引用的文献

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Endosalpingiosis of the urinary bladder: a case of probable implantative origin with characterization of benign Fallopian tube immunohistochemistry.膀胱子宫内膜异位症：一例可能起源于植入性的病例，并对良性输卵管进行免疫组织化学特征分析。
Int J Surg Pathol. 2010 Oct;18(5):381-3. doi: 10.1177/1066896909332730. Epub 2009 Mar 11.
2
Müllerianosis.苗勒管腺病
Histol Histopathol. 2007 Oct;22(10):1161-6. doi: 10.14670/HH-22.1161.
3
Tumor-like manifestation of endosalpingiosis in uterus: a case report.
Pathol Res Pract. 2005;201(7):527-30. doi: 10.1016/j.prp.2005.04.010.
4
Mullerianosis of the mesosalpinx: a case report.输卵管系膜苗勒管瘤病：一例报告
Int J Gynecol Pathol. 2003 Apr;22(2):209-12. doi: 10.1097/00004347-200304000-00018.
5
Mullerianosis of inguinal lymph nodes: report of a case.腹股沟淋巴结苗勒管瘤病：一例报告
Int J Gynecol Pathol. 2002 Jan;21(1):60-4. doi: 10.1097/00004347-200201000-00011.
6
Florid cystic endosalpingiosis of the uterus.子宫的 florid 囊性输卵管内膜异位症
J Clin Pathol. 2001 May;54(5):399-400. doi: 10.1136/jcp.54.5.399.
7
Florid cystic endosalpingiosis with tumor-like manifestations: a report of four cases including the first reported cases of transmural endosalpingiosis of the uterus.具有肿瘤样表现的 florid 囊性输卵管内膜异位症：四例报告，包括首例报道的子宫壁间输卵管内膜异位症病例。
Am J Surg Pathol. 1999 Feb;23(2):166-75. doi: 10.1097/00000478-199902000-00005.
8
Müllerianosis of the urinary bladder.膀胱苗勒管残余症
Mod Pathol. 1996 Jul;9(7):731-7.
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The secondary Müllerian system.
Obstet Gynecol Surv. 1972 Mar;27(3):133-46. doi: 10.1097/00006254-197203000-00001.

子宫多房性囊性苗勒管病：一例报告。

Multiloculated cystic Mullerianosis of uterus: A case report.

作者信息

Jayalakshmy Pattomthadathil Sankaran, Velusamy Shasi, Augustine Joy

机构信息

Department of Pathology, Government Medical College Thrissur, Kerala, India.

出版信息

J Turk Ger Gynecol Assoc. 2014 Aug 8;15(3):197-200. doi: 10.5152/jtgga.2014.76736. eCollection 2014.

DOI:10.5152/jtgga.2014.76736
PMID:25317049
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4195331/
Abstract

We are reporting a case of Mullerianosis, which presented as a multiloculated cystic mass on the serosal surface of the fundus of the uterus. Clinically and radiologically, this was interpreted as an ovarian tumor. Mullerianosis is a very rare benign tumor-like lesion. Awareness of this lesion is necessary to avoid misdiagnosis by clinicians, radiologists, and pathologists.

摘要

我们报告一例苗勒管瘤病，其表现为子宫底部浆膜表面的多房性囊性肿块。在临床和放射学上，这被误诊为卵巢肿瘤。苗勒管瘤病是一种非常罕见的良性肿瘤样病变。临床医生、放射科医生和病理科医生必须了解这种病变，以避免误诊。