Septic shock, hypercalcemia and hemophagocytic syndrome due to paracoccidioidomycosis in a 3-year-old girl

被引:0
|
作者
Rodriguez-Portilla, Ricardo [1 ]
Freundt-Thurne, Angela Parra del Riego [2 ]
Tokumura-Tokumura, Carmen Carolina [3 ]
Rojas-Soto, Ninoska Julia [3 ]
Valdes-Gomez, Jorge [4 ]
机构
[1] Clin San Felipe, Med Pediatr Intensivista, Lima, Peru
[2] Nicklaus Childrens Hosp, Dept Educ Med, Med Cirujana, Miami, FL USA
[3] Clin San Felipe, Med Hematol Pediatr, Lima, Peru
[4] Inst Patol & Biol Mol Arias Stella, Med Patol, Lima, Peru
来源
REVISTA DEL CUERPO MEDICO DEL HOSPITAL NACIONAL ALMANZOR AGUINAGA ASENJO | 2021年 / 14卷 / 03期
关键词
Paracoccidioidomycosis; Shock; Septic; Hypercalcemia; Lymphohistiocytosis; Hemophagocytic; Child; Preschool;
D O I
10.35434/rcmhnaaa.2021.143.1259
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objetive: Report the case of a girl who presented septic shock, hypercalcemia and hemophagocytic syndrome due to paracoccidioidomycosis. Case report: 3-year-old female patient with 2-month illness characterized by fever, lymphadenopathy, weight loss, abdominal distention, and severe anemia. She arrived in poor general condition, developed septic shock and a hemophagocytic syndrome. The hypercalcemia and dermal lesions were striking. A cervical ganglion biopsy and bone marrow aspirate were performed. In the latter, images compatible with Paracoccidioides were found, which were then confirmed with Grocott's stain. She was treated with amphotericin B and trimethoprim-sulfamethoxazole. The evolution was favorable and serum calcium came back to normal ranges. Conclusion: Complications caused by paracoccidioidomycosis are rare; however, the epidemiological history and bone marrow aspirate should guide the diagnosis and allow prompt treatment.
引用
收藏
页码:375 / 378
页数:4
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