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1.
J Emerg Med ; 50(5): e223-6, 2016 May.
Artigo em Inglês | MEDLINE | ID: mdl-26924510

RESUMO

BACKGROUND: Fat embolism syndrome is the result of systemic manifestations of fat emboli in the microcirculation. Duchenne muscular dystrophy is a condition that increases the risk of fracture resulting in fat emboli. CASE REPORT: We describe a patient with Duchenne muscular dystrophy who exhibited cardiopulmonary, neurologic, and ophthalmologic sequelae consistent with fat emboli syndrome after minor trauma. WHY SHOULD AN EMERGENCY PHYSICIAN BE AWARE OF THIS?: Fat embolism syndrome is a rare but important consideration with significant morbidity and risk of mortality in patients with Duchenne muscular dystrophy after even minor trauma. Early recognition and aggressive resuscitation are crucial to positive clinical outcomes.


Assuntos
Embolia Gordurosa/diagnóstico , Embolia Gordurosa/etiologia , Embolia Gordurosa/fisiopatologia , Distrofia Muscular de Duchenne/complicações , Adolescente , Diagnóstico Diferencial , Serviço Hospitalar de Emergência/organização & administração , Humanos , Masculino , Distrofia Muscular de Duchenne/fisiopatologia , Obesidade/complicações , Obesidade/fisiopatologia , Fraturas da Tíbia/complicações , Fraturas da Tíbia/fisiopatologia , Ferimentos e Lesões/complicações , Ferimentos e Lesões/fisiopatologia
2.
Mycoses ; 56(5): 596-600, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23582018

RESUMO

Tinea capitis in postpubertal patients is unusual and may be misdiagnosed as dissecting cellulitis. We report a case of a healthy 19-year-old Hispanic male presenting with a 2-month history of a large, painful subcutaneous boggy plaque on the scalp with patchy alopecia, erythematous papules, cysts and pustules. Although initially diagnosed as dissecting cellulitis, potassium hydroxide evaluation (KOH preparation) of the hair from the affected region was positive. A punch biopsy of the scalp demonstrated endothrix consistent with tinea capitis, but with a brisk, deep mixed inflammatory infiltrate as can be seen with chronic dissecting cellulitis. Fungal culture revealed Trichophyton tonsurans, and a diagnosis of inflammatory tinea capitis was made. The patient was treated over the course of 17 months with multiple systemic and topical antifungal medications, with slow, but demonstrable clinical and histopathological improvement. A rare diagnosis in adults, clinicians should have a high index of suspicion for this condition in an adult with an inflammatory scalp disorder not classic for dissecting cellulitis or with a recalcitrant dissecting cellulitis. Prompt, appropriate diagnosis and treatment is necessary to prevent the long-term complications of scarring alopecia.


Assuntos
Celulite (Flegmão)/patologia , Couro Cabeludo/patologia , Tinha do Couro Cabeludo/diagnóstico , Tinha do Couro Cabeludo/patologia , Trichophyton/isolamento & purificação , Antifúngicos/uso terapêutico , Biópsia , Histocitoquímica , Humanos , Masculino , Tinha do Couro Cabeludo/tratamento farmacológico , Adulto Jovem
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