ABSTRACT
Female patient, 42-years-old, complaining of difficulty in urinating and swelling in the vulvar area for one year. Her gynecological examination showed extensive injury in the vulvar region and the biopsy done was inconclusive. The removal of the lesion was conducted. After the procedure, the patient remains free of recurrence for 15 months. This case highlights the need to consider angiomyxoma in the differential diagnosis for tumors of unknown cause in the vulvar region.
Paciente do gênero feminino, 42 anos, com queixas de dificuldade ao urinar e aumento de volume na região vulvar há 1 ano. Ao exame ginecológico, apresentava extensa lesão na região vulvar. Biópsia da lesão foi inconclusiva. Realizou-se a exérese da lesão. A paciente permanece livre de recorrências há 15 meses. Este caso destaca a necessidade de considerar o angiomixoma no diagnóstico diferencial de massas de causa desconhecida na região vulvar.
Subject(s)
Adult , Female , Humans , Myxoma/pathology , Vulva/pathology , Vulvar Neoplasms/pathology , Biopsy , Diagnosis, Differential , Myxoma/surgery , Stromal Cells/pathology , Tomography, X-Ray Computed , Treatment Outcome , Vulvar Neoplasms/surgeryABSTRACT
Although cryptococcal infections begin in the lungs, meningoencephalitis is the most frequently encountered manifestation of cryptococcosis among individuals with advanced immunosuppression. As the infection progresses along the Virchow-Robin spaces, these structures may become dilated with mucoid material produced by the capsule of the organism. We report a case of a 24-year-old man with cryptococcal meningoencephalitis in which magnetic resonance imaging showed clusters of gelatinous pseudocysts in the periventricular white matter, basal ganglia, mammillary bodies, midbrain peduncles and nucleus dentatus with a soap bubble appearance.
Subject(s)
Humans , Male , Young Adult , Cryptococcosis/diagnosis , Magnetic Resonance Imaging , Meningoencephalitis/diagnosis , Artifacts , Meningoencephalitis/microbiologyABSTRACT
Os autores relatam o caso de uma mulher de 50 anos de idade que procurou auxílio médico referindo aumento do volume abdominal há 8 meses. Negava quaisquer outros sintomas. Tomografia computadorizada do abdome mostrou lesão sólida retroperitoneal medindo aproximadamente 6 por 5,2 cm na região inter-aórtico-caval. A biópsia percutânea da lesão revelou tratar-se de neoplasia indiferenciada compatível com feocromocitoma extra-adrenal. A paciente submeteu-se a laparotomia com resseção completa da lesão. O exame histopatológico do espécime cirúrgico foi compatível com paraganglioma. A paciente está bem e sem evidências de recidiva da doença 9 meses após a operação.
Subject(s)
Middle Aged , Female , Humans , Paraganglioma , Paraganglia, Chromaffin/pathology , PheochromocytomaABSTRACT
CONTEXT: Meigs' syndrome consists of a benign ovarian tumor accompanied by ascites and hydrothorax. Elevated serum CA 125 levels in postmenopausal women with solid adnexal masses, ascites and pleural effusion are highly suggestive for malignant ovarian tumor. However, patients with Meigs' syndrome can also have elevated serum CA 125 levels. The authors report a case of Meigs' syndrome with elevated CA 125 level. OBJECTIVE: This is a case report of Meigs' syndrome with elevated CA 125 level. CASE REPORT: A 65-year-old Brazilian woman had presented progressive dyspnea, weight loss and decline in general condition over the 7 months preceding admission to our service. In another hospital, the patient had been submitted to thoracic drainage due to pleural effusion. With recurrence of the pleural effusion and increase in abdominal volume due to ascites and a pelvic mass, the patient sought our service. Transvaginal ultrasound showed an extensive adnexal solid mass of 16.4 x 10.8 cm located in the pelvis without exact limits, and the serum CA 125 level was elevated. With a preoperative diagnosis of ovarian carcinoma, the patient was submitted to exploratory laparotomy, which revealed a left ovarian tumor. The frozen section diagnosis was thecoma. Total abdominal hysterectomy with bilateral salpingo-oophorectomy was performed. The histology of the specimen confirmed the diagnosis of thecoma. The patient was asymptomatic with a normal serum CA 125 level 20 months after the operation