Epithelioid leiomyosarcoma of uterine cervix: A case report with immunohistochemical study

نویسنده

  • Tadashi Terada
چکیده

Primary epithelioid leiomyosarcoma of uterine cervix (UC) has rarely been reported. A 90-year-old woman presented abnormal uterine bleedings. Colposcopy revealed erosions of cervix, and biopsy was taken. It showed proliferation of atypical spindle and epithelioid cells with hyperchromatic nuclei and prominent nucleoli. Mitotic figures including atypical mitosis were noted. The histological features were apparent malignancy. The gradual merges between epitheliod malignant cells and malignant spindle cells were seen. Immunohistochemically, both elements (spindle and epithelioid) were positive for vimentin, α-smooth muscle actin, smooth muscle actin (HHF-35), h-caldemon, cytokeratin (CK) AE1/3, CK CAM5.2, CK WSS, CK8, CK18, CK19, p53 and Ki67 (labeling index = 57%). They were negative for S100 protein, NSE, NCAM, synaptophysin, chromogranin, desmin, CK34BE12, CK5, CK6, CK7, CK14, CK20, CD1a, CD99, CD31, factor VIII-related antigen, CD34, HMB45, KIT, PDGFRA, CA125, CA19-9, CEA, bcl-2, CD3, CD20, CD45, CD138, and myoglobin. The tumor histologically showed epithelioid and mesenchymal features, and immunohistochmeically the tumor was positive for vimentin, smooth muscle markers, and CK. The following three possibilities of pathological diagnosis were considered; epithelioid leiomyoma, sarcomatoid carcinoma, and epithelioid carcinoma. The author stressed the expressions of various smooth muscle antigens, and diagnosed this tumor as epithelioid leiomyosarcoma. The patient refused operation and chemo-radiation. The patient showed no metastatic lesions, but died of pneumonia three years after the diagnosis at the age of 93 years. This is a rare case report of epithelioid leiomyosarcoma in UC.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Two cases of perivascular epithelioid cell tumor of the uterus: clinical, radiological and pathological diagnostic challenge

BACKGROUND Perivascular epithelioid cell tumor (PEComa) is a rare subtype of mesenchymal origin tumor composed of epithelioid cells which exhibits immunohistochemical co-expressions of melanocytic markers and smooth muscle markers. CASE PRESENTATION In the first case, malignant uterine PEComa with vaginal and multiple lung metastasis was misdiagnosed preoperatively as uterine leiomyosarcoma d...

متن کامل

Uterine epithelioid leiomyosarcoma with c-kit expression and YWHAE gene rearrangement: a case report of a diagnostic pitfall of uterine sarcoma

BACKGROUND Uterine sarcoma is a rare tumor that is often difficult to classify based on morphological and immunohistochemical analysis alone. Limited access to molecular biological analysis in routine practice would hinder making a definitive diagnosis. CASE PRESENTATION In this report, we describe a case of a mesenchymal tumor arising from the uterine cervix in a 52-year-old woman. From micr...

متن کامل

Leiomyosarcoma with Unusual Macroscopic Features: A Case Report

Uterine sarcoma is a rare tumor of mesodermal origin, accounting for 2-6% of uterine malignancies. Leiomyosarcoma (LMS) has been reported in only 1% of all uterine malignancies and is regarded as the most common primary uterine sarcoma. Herein, we present a case of LMS with unusual macroscopic features. The patient was a 61-year-old woman with LMS, which consisted of a large cystic mass (88×136...

متن کامل

Malignant perivascular epithelioid cell tumor (PEComa) of the uterus with late renal and pulmonary metastases: a case report with review of the literature

BACKGROUND Perivascular epithelioid cell tumor (PEComa), other than angiomyolipoma (AML), clear cell sugar tumor (CCST), and lymphangioleiomyomatosis (LAM), is a very rare mesenchymal tumor with an unpredictable natural history. The uterus is the most prevalent reported site of involvement of PEComa-not otherwise specified (PEComa-NOS). To the best of our knowledge, about 100 PEComa-NOS have be...

متن کامل

Cervical Leiomyosarcoma: A Case Report

Introduction: Sarcoma of the cervix is uncommon and its prevalence is about 1% of malignancies of the cervix. One type of sarcoma is leiomyosarcoma and the location of this tumor in cervix is very rare. Although uterine sarcoma can involve the cervix and lead to misdiagnosis of cervical leiomyosarcoma, the location of the bulk of the tumor in uterine cervix (not isthmus) for diagnosis of cervic...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2016