Primary Leiomyosarcoma Of Kidney In A Young Adult

Primary renal leiomyosarcoma (LMS) is an extremely rare tumor constituting to <2% of all malignant renal tumors. Here, we present the case of a 28-year-old female with a right lower polar renal tumor, who underwent partial nephrectomy which on microscopy suggested LMS. Due to the lack of a follow-up protocol and low survival rates, regular imaging and a multidisciplinary approach were considered in the patient

Extranodal non-Hodgkin's lymphoma presenting as an ovarian mass.

An 8-year-old female presented with an abdominal lump. A ultrasonography showed a heterogeneous, mainly solid space-occupying lesion with few cystic components and irregular margin in both adnexae measuring 10.5 x 5.2 x 3.5 cm and 9.2 x 4.8 x 3.0 cm. The tumors were removed by exploratory laparotomy and the histopathological report was primary NHL of the ovary. The uterus and cervix were healthy and there was no tumor extension or omental deposit. The patient was referred for chemotherapy.

Coexistence of a mature teratoma and mucinous cystadenocarcinoma in the same ovary--a case report.

A case of right sided abdominal lump with pain in a 45 years female was presented. Radiological investigation revealed a multiloculated cystic mass with a few mural nodules arising from right ovary. The tumor was removed by exploratory laparotomy and histopathological examination showed coexistence of dermoid cyst with mucinous cystadenocarcinoma in the same ovary. Left ovary and uterus was healthy and there was no tumor extension or omental deposits. Postoperative period was uneventful.