SUMMARYIntroduction: We present a fatal case of disseminated cryptococcosis in a young man whose diagnosis of HIV infection was made at the time of admission to the emergency room. Case report: The patient was a twenty-three-year-old man, with a history of daily fever during one month associated with diarrhea, weight loss, headache, vomiting and generalized seizures. He also had a history of diabetes mellitus, alcoholism and drug addiction. Upon physical examination the patient was pale, disoriented and had periods of agitation. White blood cells count was 3,440/mm3 (5% lymphocytes), hemoglobin was 10g/dL, platelets were 83,000/ mm3. Creatinine was 0.7 mg/dL; urea 19 mg/dL; Na, K, and liver enzymes were within normal limits. Lactic dehydrogenase was 494 IU/L. Cerebrospinal fluid (CSF) analysis revealed 10 white blood cells/mm3 (58% neutrophils, 31% lymphocytes, 11% monocytes) and 2 red blood cells/mm3. India ink test revealed six Cryptococcus yeasts/mm3. CSF glucose was 122 mg/dL and protein was 36 mg/ dL. VDRL test was negative and anti-HIV test was positive. Intravenous hydration, insulin, phenytoin, fluconazole, pyrimethamine, sulfadiazine, folinic acid, and amphotericin B were started. The patient did not improve and became obtunded and hypotensive. He was intubated and put on mechanical respiration. He received vasoactive drugs and died less than 24 hours after admission. A postmortem examination was performed and revealed disseminated cryptococcosis, with severe involvement of the kidneys. Conclusion: Cryptococcosis, as a rule, is a systemic disease that affects mostly immunocompromised individuals, especially patients with AIDS. When diagnosed late in its course it has a very high mortality.
O tumor epitelial e estromal misto do rim é uma neoplasia rara, caracterizada pelo seu padrão histopatológico bifásico, formado por elementos epiteliais e estromais. Predomina no sexo feminino, na perimenopausa e sua patogênese ainda é desconhecida. Relata-se o caso de uma paciente de 54 anos, que iniciou crises recorrentes de dor em flanco direito e disúria. Os exames de imagem evidenciaram lesão cística complexa em rim esquerdo e paciente foi submetida à nefrectomia. O exame histopatológico e a imuno-histoquímica confirmaram o diagnóstico.
A nefropatia diabética (ND) é atualmente a principal causa da doença renal em estágio terminal (DRET), na Europa e Estados Unidos, e a segunda causa, no Brasil. A recorrência histológica da nefropatia diabética tem sido descrita em cerca de 40% dos pacientes, sendo o diagnóstico de recorrência realizado em média de 6-8 anos pós-transplante renal, mas, com relatos de recorrência tão precoce como dois anos. Relatamos o caso de um paciente com diagnóstico prévio de diabetes mellitus que foi submetido a transplante renal com doador falecido e evoluiu à recorrência de nefropatia diabética, no primeiro ano após transplante, com diagnóstico de certeza, somente após biópsias repetidas.
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