RESUMO
ABSTRACT Brazilian spotted fever, a zoonotic disease transmitted by ticks, is caused by Rickettsia rickettsii. We report a fulminant case of this zoonosis in a healthy 46-year-old military man in the urban region of Rio de Janeiro city, in October, 2021. Ticks and capybaras (Amblyomma sculptum, Hydrochoerus hydrochaeris, respectively) were identified in the military fields, pointing to the participation of this large synanthropic rodent, recognized as an efficient amplifier host of Rickettsia rickettsii in Brazil. As the military population is considered a risk group for spotted fever, it is necessary to alert health professionals to the importance of the early detection of the disease and its adequate management, mainly in populations that are particularly at risk of exposure to ticks, in order to avoid fatal outcomes.
RESUMO
Síndrome LPAC (Low Phospholipid-Associated Cholelithiasis) é uma enfermidade rara, que cursa com manifestações clínicas recorrentes relacionadas à litíase biliar, mesmo após colecistectomia em indivíduos jovens habitualmente com início dos sintomas antes dos 40 anos. Mutações no gene ABCB4 geram baixa concentração de fosfolipídios na secreção biliar, o que favorece a formação de cálculos de colesterol. Seu diagnóstico é estabelecido por critérios clínicos e o tratamento é fundamentado no uso do ácido ursodesoxicólico (UDCA). O objetivo deste artigo é relatar o caso de um paciente com síndrome LPAC.
Achalasia is an uncommon disorder that affects about LPAC syndrome (Low phospholipid-associated cholelithiasis) is a rare illness that leads to recurrent clinical manifestations related to gallstones, even after cholecystectomy in young individuals, usually with onset of symptoms before age 40. Mutations in the gene ABCB4 generate low concentration of phospholipids in bile secretion, which promotes the formation of cholesterol calculations. The diagnosis is established by clinical criteria and treatment is based on the use of ursodeoxycholic acid (UDCA). The objective of this paper is to report the case of a patient with LPAC syndrome.