Endometrial Stromal Sarcoma Recurrence in the Caecum
نویسندگان
چکیده
منابع مشابه
Primary Stromal Sarcoma of Breast with Nodal Recurrence
Although most breast cancers are adenocarcinomas of the mammary gland, primary breast sarcomas may also arise from mammary gland mesenchymal tissue. Sarcomas represent less than 1% of primary breast neoplasms. These tumors are at high risk of recurrence and are known to have poor prognosis. Surgical resection is the primary treatment for these lesions and axillary lymph node dissection is no...
متن کاملLow Grade Endometrial Stromal Sarcoma: A Case Report
Endometrial stromal sarcoma (ESS) is a rare malignant tumor of the endometrium, occurring in the age group of 40–50 years. We report a case of low-grade ESS in a 39-year-old woman, presenting as rapid enlargement of a uterine fibroid polyp associated with irregular and excessive vaginal bleeding. Polypectomy followed by pan hysterectomy was performed. Histopathological examination and immunohis...
متن کاملEndometrial stromal sarcoma arising in vagina.
Endometrial stromal sarcoma (ESS) arising in the vagina is an extremely rare extrauterine endometrial stroma sarcoma, with only 4 cases reported in the literature up to date. Here we report a case of neoplasm originating from vagina. A 32-year-old woman complained of intermittent vaginal bleeding especially after intercourse. A mass with a diameter of 1.0 cm was found in the middle and upper se...
متن کاملEndometrial stromal sarcoma in combination with mixed type endometrial carcinomas
RATIONALE Endometrial stromal sarcoma (ESS) is rare, representing only approximately 0.2% of all uterine malignancies. Mixed type endometrial carcinomas (MT-ECs) are rare tumors with both type I and II features, and are difficult to diagnose. Cases of ESS and MT-ECs coexisting in the same patient are extremely rare. This study aimed to describe a case of ESS in combination with MT-ECs in a 47-y...
متن کاملSuccessful Pregnancy with Endometrial Stromal Sarcoma (ESS).
Endometrial stromal sarcoma (ESS) is very rare malignant tumor that constitutes approximately 10 % of all uterine sarcomas but only 0.2 % of all uterine malignancies [1]. ESS can be mistaken for leiomyoma because clinical presentation mimics each other and often needs HPE to establish correct diagnosis [2, 3]. In this article, we report a case of ESS in a young unmarried female of 23 years, whi...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Case Reports in Surgery
سال: 2018
ISSN: 2090-6900,2090-6919
DOI: 10.1155/2018/9139281