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1.
BMJ Case Rep ; 16(7)2023 Jul 18.
Artículo en Inglés | MEDLINE | ID: mdl-37463776

RESUMEN

Coccidioidomycosis is known to occur around the western hemisphere. In tropical countries, the clinical presentation is atypical presenting with a superficial abscess preceded by respiratory tract involvement often mimicking tuberculosis. Eliciting a history of exposure and high suspicion is imperative for early diagnosis.In the present case report, a man in his early 30s presented with complaints of swelling over the neck for the past 2 months with a recent travel history. With a provisional clinical diagnosis of tuberculosis, a biopsy of the swelling revealed features of granulomas with non-caseating necrosis with Coccidioidomycosis organisms demonstrated by fungal stains. Fungal culture and serology reiterated Coccidioides and he recovered after a course of fluconazole.The case report concludes with a statement that Coccidioidomycosis is known to manifest with lymphadenitis mimicking tuberculosis and must be taken into account as one of the differentials. The current report is presented for its rarity in India with atypical presentation.


Asunto(s)
Coccidioidomicosis , Linfadenopatía , Masculino , Humanos , Coccidioidomicosis/diagnóstico , Coccidioidomicosis/tratamiento farmacológico , Coccidioidomicosis/microbiología , Antifúngicos/uso terapéutico , Fluconazol/uso terapéutico , Coccidioides , Linfadenopatía/tratamiento farmacológico
2.
Indian J Pathol Microbiol ; 63(4): 611-614, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-33154316

RESUMEN

Granulomatosis with polyangiitis (GPA) is a systemic necrotizing vasculitis involving small and medium-sized blood vessels and granulomatous inflammation of upper and lower respiratory systems and/or renal system. In the limited form of GPA, there is no systemic involvement of disease with sparing of kidneys. The respiratory system is the commonly involved organ in limited GPA. Herein, we report the case of a 40-year-old male who was initially diagnosed as sarcoidosis clinically. Lung biopsy revealed necrotizing granulomatous angiitis. Diagnosis of GPA was made which was substantiated by antineutrophil cytoplasmic antibody (ANCA) positivity. This was a case of limited GPA with isolated lung involvement. The early diagnosis and initiation of treatment are critical for improved survival of patients with GPA. Tissue biopsy is necessary for the diagnosis of GPA.


Asunto(s)
Granulomatosis con Poliangitis/diagnóstico , Pulmón/patología , Adulto , Anticuerpos Anticitoplasma de Neutrófilos/inmunología , Biopsia , Granulomatosis con Poliangitis/inmunología , Granulomatosis con Poliangitis/patología , Humanos , Inflamación , Masculino
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