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1.
Oxf Med Case Reports ; 2019(8): omz081, 2019 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-31772748

RESUMO

Gastric cancer represents the fifth most common cancer diagnosis worldwide and the third leading cause of cancer-related mortality. In the USA, the overall 5-year survival rate is 31%, with distant disease nearing 5%. The most common sites of metastasis are the liver and peritoneum. Skeletal muscle involvement has been rarely reported. Since clinical and imaging findings overlap with primary sarcomas, a confirmatory biopsy is required for diagnosis. Prognosis remains poor with treatment options including palliative chemotherapy, radiotherapy and surgical resection. We report the case of a 57-year-old female presenting with extensive involvement of skeletal muscle 10 years after achieving remission. In addition to illustrating the refractoriness and poor outcomes associated with muscle involvement, this case and comprehensive review of the literature highlights important characteristics of disease biology and tumor genomics that warrant detailed discussion and exposition to a wider audience.

2.
Transplant Proc ; 49(2): 373-377, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28219601

RESUMO

Syndrome of inappropriate anti-diuretic hormone (SIADH) has been reported to be associated with systemic Strongyloides stercoralis. Here, we report a case of a stem cell transplant (SCT) recipient who developed severe SIADH secondary to systemic S Stercoralis. The SIADH resolved quickly after treating the systemic S Stercoralis with ivermectin. A systematic review of the literature was performed by PubMed, Scopus, and Cochrane database search. Only eight cases of S Stercoralis in allogeneic SCT recipients have been previously reported. To our knowledge, ours is the first reported case of SIADH secondary to S Stercoralis infection in an allogeneic SCT recipient. Prior to transplantation, even if asymptomatic, patients from endemic regions should be screened with strongyloides immunoglobulin (Ig)G serology. Pretransplantation eosinophilia should be evaluated by screening multiple stool samples for ova and parasites. Transplant candidates with positive serology or stool tests can be treated pretransplantation to eradicate infection. Patients at risk for S Stercoralis who develop nonspecific gastrointestinal complaints, rash, pulmonary infiltrates, or gram-negative bacteremia or meningitis may have S Stercoralis hyperinfection syndrome. Our case indicates that the development of SIADH may be an additional clue to this diagnosis. Appropriate diagnostic studies, including repeat stool and other body fluid sampling, should be expedited and ivermectin therapy initiated rapidly to prevent significant morbidity and mortality.


Assuntos
Duodenopatias/parasitologia , Síndrome de Secreção Inadequada de HAD/parasitologia , Infecções Oportunistas/complicações , Transplante de Células-Tronco , Strongyloides stercoralis , Estrongiloidíase/complicações , Idoso , Animais , Antinematódeos/efeitos adversos , Antinematódeos/uso terapêutico , Duodenopatias/tratamento farmacológico , Eosinofilia/parasitologia , Humanos , Imunoglobulina G/sangue , Ivermectina/uso terapêutico , Masculino , Infecções Oportunistas/tratamento farmacológico , Complicações Pós-Operatórias/tratamento farmacológico , Complicações Pós-Operatórias/parasitologia , Transplante Homólogo
4.
Pediatr Transplant ; 17(2): E55-61, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23230886

RESUMO

BKV is known to cause allograft failure in kidney transplant recipients. It has been recently recognized to cause native kidney nephropathy in non-kidney transplant recipients. This is a case report BKVN in a 15-yr-old HTx recipient who had PTLD and a review of pediatric cases in the literature. The patient was diagnosed with BKVN +189 months after transplantation and died thirty days after diagnosis of BKVN. We identified five other cases of BKVN in pediatric non-kidney solid organ transplantation, of which all were HTx recipients. Overall, outcome was poor and BKV clearance was not achieved with reduction of immunosuppression and with current therapies. We strongly recommend that pediatric HTx recipients be tested for BKV infection if there is evidence of kidney dysfunction. We also recommend that they have an annual screening for BKV viruria and viremia with the assessment of kidney function.


Assuntos
Vírus BK , Transplante de Coração , Nefropatias/diagnóstico , Linfoma de Células T Periférico/diagnóstico , Infecções por Polyomavirus/diagnóstico , Complicações Pós-Operatórias/diagnóstico , Infecções Tumorais por Vírus/diagnóstico , Adolescente , Vírus BK/isolamento & purificação , Evolução Fatal , Humanos , Nefropatias/etiologia , Nefropatias/virologia , Linfoma de Células T Periférico/etiologia , Masculino , Infecções por Polyomavirus/etiologia , Complicações Pós-Operatórias/virologia , Infecções Tumorais por Vírus/etiologia
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