Imaging of an exceptional urinoma complicating a cervical cancer and leading to death: A case report.

Spontaneous urinoma is a rare urological complication that can occur following acute urinary obstruction. It involves a collection of urine that typically forms around the kidney as a result of rupture of the fornix. There are several causes of acute urinary stasis, including lithiasis, tumors, prostatic hypertrophy, and others. We present a unique case of an asymptomatic spontaneous urinoma discovered incidentally during the extension study of a 66-year-old woman with cervical cancer. The positive diagnosis was made through a combination of ultrasound and uro-computed tomography scan. The evolution was marked by the occurrence of a uremic encephalopathy, leading to death before any treatment.

Primary rectal adenocarcinoma with musculoskeletal metastasis as the only metastasis site: A case report with a short literature review.

Rectal carcinoma with metastasis to skeletal muscle is a rare occurrence. Since 1970, only 30 cases of skeletal muscle metastasis originating from colorectal adenocarcinomas have been documented, underscoring its exceptionally low incidence. Here, we present the case of a middle-aged man who was diagnosed with rectal adenocarcinoma 3 months ago. During examination, a subcutaneous mass was discovered in the left proximal buttock. Histological analysis of a biopsy confirmed that this mass was a metastatic lesion originating from the primary rectal adenocarcinoma.

Primary cutaneous adenoid cystic carcinoma with lung metastasis: A case report with literature review.

Adenoid cystic carcinoma is a rare tumor that typically originates from secretory glands, most commonly found in the salivary glands. However, it can also develop as a primary cutaneous adenoid cystic carcinoma, which appears identical under the microscope to adenoid cystic carcinoma originating in other tissues. Distinguishing between primary cutaneous adenoid cystic carcinoma and extracutaneous adenoid cystic carcinoma with cutaneous metastases is crucial for determining the prognosis and appropriate management of the condition. In this case report, we describe a case of primary cutaneous adenoid cystic carcinoma located on the hand with lung metastases. Proper differentiation, treatment planning and regular clinical follow-up to monitor for any signs of recurrence or metastasis are essential to ensure favorable outcomes for patients with this rare neoplasm.

Splenic metastasis from neuroendocrine tumor of the stomach: A case report.

Splenic metastasis is extremely rare, and neuroendocrine tumor of the stomach represents one of the rarest primary sources. The present study aimed to describe a rare case of an endocrine tumor of the stomach revealed by a splenic metastasis. We report a rare case of a 40 -year-old who presented a pain in her left hypochondriac, associated to sensation of heaviness. Abdominal ultrasound showed splenomegaly with a large lobulated hyperechoic mass associated to splenic vein thrombosis. A magnetic resonance imaging (MRI) confirming the splenomegaly, containing a large lobulated and heterogeneous mass occupying the almost totality of this organ and invading the venous system. The histological study of this splenic mass demonstrated to secondary splenic location of a grade 1 neuroendocrine tumor. As part of an investigation for a primary tumor, fibro scopy was performed and revealed an ulcerating-bourging fundic process with a histological study in favor of a grade 1 neuroendocrine tumor.

Fistula formation between infected pelvic lymphocele and sigmoid colon: A rare complication of pelvic lymphadenectomy.

Lymphocele formation following pelvic lymphadenectomy is a well-known complication. In this article, we report a 56 years old female patient with a pelvic infected lymphocele fistulised in the sigmoid discovered in imaging 2 months after pelvic surgery. Lymphocele complications are rare and their diagnosis is based on imaging. However, lymphocele as a potential cause for fistula in the bowel as a particular new case has not been found in literature search.