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1.
Rheumatol Int ; 42(8): 1477-1482, 2022 08.
Artigo em Inglês | MEDLINE | ID: mdl-34287686

RESUMO

Monogenic lupus is a subset of lupus caused by single-gene disorders, integrating the paradoxical combination of autoimmunity and immunodeficiency. Pulmonary manifestations with recurrent pneumonia and bronchiectasis have rarely been described as the predominant presentation of juvenile lupus and may suggest an alternate differential like primary immunodeficiency, especially in early childhood. We describe a case of 10-year girl who presented with a history of recurrent pneumonia, arthritis, alopecia, and poor weight gain for the past 2 years. On examination, she had respiratory distress, bilateral diffuse crackles and arthritis of the small joints of hands. Lab investigations showed pancytopenia, low complement levels and high titers of ANA and anti-dsDNA antibodies. The patient was diagnosed with juvenile lupus. Imaging studies revealed evidence of multiple lobar collapse and consolidation with bronchiectasis. She was started on steroids, HCQ and supportive measures for bronchiectasis. The child reported relief in initial symptoms of lupus on follow-up but developed recurrent thrombocytopenia requiring IVIG and escalating the doses of oral steroids. The young age and atypical presentation prompted a screening for monogenic lupus, and clinical exome sequencing revealed a novel homozygous missense variation in exon 20 of the C4Agene with clinically reduced C4 levels, consistent with the diagnosis of C4A deficiency.


Assuntos
Artrite , Bronquiectasia , Lúpus Eritematoso Sistêmico , Trombocitopenia , Anticorpos Antinucleares , Bronquiectasia/tratamento farmacológico , Bronquiectasia/genética , Criança , Pré-Escolar , Complemento C4a/deficiência , Feminino , Doenças da Deficiência Hereditária de Complemento , Humanos , Lúpus Eritematoso Sistêmico/complicações , Lúpus Eritematoso Sistêmico/diagnóstico , Lúpus Eritematoso Sistêmico/tratamento farmacológico , Esteroides , Trombocitopenia/etiologia , Trombocitopenia/genética
2.
Indian J Pathol Microbiol ; 63(4): 648-650, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-33154328

RESUMO

Entomophthoromycosis is a rare fungal infection of the skin and subcutaneous tissue occurring predominantly in tropical and subtropical regions. In children, it mostly affects the lower half of the body. With this, we report a case of Entomophthoromycosis in a 6-year-old girl who presented late with extensive involvement of the upper half of the body. She responded well to treatment with potassium iodide and itraconazole. We also reviewed cases of Entomophthoromycosis reported in children.


Assuntos
Diagnóstico Tardio , Pele/patologia , Zigomicose/diagnóstico , Antifúngicos/uso terapêutico , Biópsia , Criança , Feminino , Humanos , Itraconazol/uso terapêutico , Linfadenopatia/diagnóstico por imagem , Linfadenopatia/microbiologia , Iodeto de Potássio/uso terapêutico , Pele/microbiologia , Tomografia Computadorizada por Raios X , Resultado do Tratamento , Zigomicose/complicações , Zigomicose/tratamento farmacológico
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