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1.
Korean Journal of Nuclear Medicine ; : 319-323, 2020.
Artigo em Inglês | WPRIM | ID: wpr-997486

RESUMO

Although prostate cancer can metastasize to any part of the body, isolated testicular metastasis is very rare and only few cases have been reported so far. Here we present a case of 65-year-old male patient, known case of prostate adenocarcinoma, referred for 68Ga-PSMA PET/CT scan, post radiotherapy, and androgen deprivation therapy, for rising serum PSA levels. He was found to have an isolated testicular metastasis on the scan. This report highlights the importance of 68Ga-PSMA PET-CT scan in detecting these unusual and rare sites of metastasis from prostate cancer.

2.
Kidney Research and Clinical Practice ; : 287-291, 2018.
Artigo em Inglês | WPRIM | ID: wpr-717210

RESUMO

Adenine phosphoribosyltransferase enzyme deficiency is a rare, autosomal recessive disorder. It is a disease limited to the renal system and usually presents with urolithiasis. Herein, we report a young female with dihydroxyadenine (DHA) crystal-induced nephropathy presenting with rapidly progressive renal failure. DHA crystals can be easily diagnosed by their pathognomic color and shape in urine and biopsy specimens. A high index of clinical suspicion helps in the early diagnosis of this potentially treatable renal disease.


Assuntos
Feminino , Humanos , Adenina Fosforribosiltransferase , Biópsia , Diagnóstico Precoce , Insuficiência Renal , Urolitíase
3.
Anaesthesia, Pain and Intensive Care. 2013; 17 (2): 202-204
em Inglês | IMEMR | ID: emr-147585

RESUMO

We present a case of Japanese encephalopathy, which posed serious problems during diagnosis as well management. Our patient had to be nursed in ICU and mechanically ventilated for a prolonged period [more than 50 days] and was successfully weaned, but with difficulty and with sustained and careful monitoring and flexible planning. A multispecialty approach made all the difference between life and death

4.
Pan Arab Journal of Neurosurgery. 2011; 15 (1): 68-70
em Inglês | IMEMR | ID: emr-109048

RESUMO

Intraosseous haemangiomas of skull are rare neoplasms, The authors report a series of three cases of intraosseous haemangioma of skull. The clinical features, pathological findings lesions are discussed in the light of available literature

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