Persistent Mullerian Duct Syndrome with Malignant Conversion of Mullerian Remnant

Abhilasha Jain, Palak Gandhi, Jagannathan Krishnan, J. Ghetiya
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Abstract

 A case report of a very rare entity of persistent Müllerian duct syndrome with malignant transformation of Mullerian remnant is presented. A twenty-two-year-old phenotypically normal male presented with complain of hematuria and lower abdominal pain. On examination patient had bilateral cryptorchidism and on imaging bilateral duplication of pelvicalyceal system and ureters and left sided ureterocoele. There was a malignant mass lesion with metastatic lymphadenopathy in pelvis. The diagnosis of persistent Mullerian duct syndrome was suspected on MRI pelvis and confirmed by genetic and pathological testings. Risk of malignant transformation of undescended testis and Mullerian remnants increases with age and have impact on psychological health of patient, so early diagnosis becomes crucial.
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持续性苗勒管综合征伴残余苗勒管恶性转化
本文报告一例罕见的持续性勒氏管综合征伴残余勒氏管恶性转化的病例。22岁男性,表现正常,主诉血尿及下腹部疼痛。检查发现患者双侧隐睾,影像学检查发现双侧肾盂系统和输尿管重叠,左侧输尿管膨出。骨盆有恶性肿块伴转移性淋巴结病变。骨盆MRI疑似持续性苗勒管综合征,经遗传和病理检查证实。随着年龄的增长,隐睾和缪勒管残余恶性转化的风险增加,并影响患者的心理健康,因此早期诊断至关重要。
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