Severe Disseminated Phaeohyphomycosis in a Patient with Inherited CARD9 Deficiency
نویسندگان
چکیده
منابع مشابه
Disseminated phaeohyphomycosis in a dog
Phaeohyphomycosis is a rare but emerging disease caused by dematiaceous fungi. Here we describe the case of an immunosuppressed dog with disseminated phaeohyphomycosis secondary to Bipolaris spicifera infection. Regionally extensive infiltration of the paw pads, skin, myocardium, liver, renal interstitium and diaphragm was identified on histopathology. Candida glabrata and Fusarium oxysporum we...
متن کاملInherited CARD9 deficiency in 2 unrelated patients with invasive Exophiala infection.
BACKGROUND Exophiala species are mostly responsible for skin infections. Invasive Exophiala dermatitidis disease is a rare and frequently fatal infection, with 42 cases reported. About half of these cases had no known risk factors. Similarly, invasive Exophiala spinifera disease is extremely rare, with only 3 cases reported, all in patients with no known immunodeficiency. Autosomal recessive CA...
متن کاملDisseminated subcutaneous phaeohyphomycosis caused by Exophiala oligosperma in a patient with Wegener's granulomatosis.
Takanobu Kan'", Shun$uke Takahagi'", Akiko Kamegashira', Hiroshi Ooiwa^ Takashi YaguchP and Michihiro Hide'* 'Department of Dermatology, Programs for Biomédical Researcii, Division of Molecular Medicai Science, Graduate School of Biomédical Sciences, -Department of Clinicai Immitnoiogy and Rlieumatology, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8551, and ^Medical Mycology Re...
متن کاملDisseminated BCG Infection in a patient with Severe Combined Immunodeficiency
Disseminated mycobacterial infection after bacillus Calmette-Guerin (BCG) vaccination is a very rare disorder, occurring mostly in patients with immunologic deficiency. We report a case of disseminated BCG infection in a 16-month-old girl with severe combined immunodeficiency. Plain radiographs showed multiple osteolytic lesions in the femora, tibiae, humerus, and phalanges. Abdominal sonograph...
متن کاملInherited apolipoprotein A-V deficiency in severe hypertriglyceridemia.
OBJECTIVE Mutations in LPL or APOC2 genes are recognized causes of inherited forms of severe hypertriglyceridemia. However, some hypertrigliceridemic patients do not have mutations in either of these genes. Because inactivation or hyperexpression of APOA5 gene, encoding apolipoprotein A-V (apoA-V), causes a marked increase or decrease of plasma triglycerides in mice, and because some common pol...
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ژورنال
عنوان ژورنال: Archives of Clinical Infectious Diseases
سال: 2018
ISSN: 2345-2641
DOI: 10.5812/archcid.84006