Cryptococcal cellulitis in a patient with bullous pemphigoid.
نویسندگان
چکیده
Cryptococcosis is a rare, life-threatening fungal infection caused by the yeast-like encapsulated fungus Cryptococcus neoformans. It is considered an opportu-nistic infection as it affects mainly immunosuppressed individuals (1, 2). The disease is believed to be acquired mainly by inhalation of the infectious propagule from the environment. In humans, C. neoformans causes various kinds of clinical manifestations; meningoencephalitis, pneumonia, skin lesions, eye lesions, bone involvement, etc. (3). AIDS is the predisposing factor in approximately 90% of cryptococcal infections (4). Other defects in T-cell-mediated immunity are also predisposing factors of infection, such as haematological malignancies (4). We report here an elderly male patient with bullous pemphigoid (BP) who was complicated with cryptococ-cal cellulites. A 79-year-old man, living in a big city in Japan, presented with swelling, erythema and severe pain of the left arm. The skin lesions had developed rapidly. The patient reported an accidental injury of the left arm before the skin lesions. The patient had had BP for one year and had been treated with oral prednisolone at 17.5 mg daily from the onset of the lesion on the arm. The diagnosis of BP was based on skin manifestations of generalized multiple bullae (Fig. 1), histological features of subepidermal blisters with eosinophilic infiltration, deposition of IgG and C3 at the dermal basement membrane zone, and high-titre circulating anti-BP180 antibodies detected with BP180 enzyme-linked im-munoassay (ELISA) (MBL Intl. Corp., Nagoya, Japan). On examination, the left forearm exhibited swelling and ery-thema, suggesting cellulitis. The left axillary lymph nodes were palpable. The results of blood examination were as follows: white blood cell count of 11,600/µl (normal: 4,000–8,000/µl), C-reactive protein of 6.77 mg/dl (< 0.30 mg/dl), urea nitrogen of 30 mg/ dl (10–15 mg/dl), creatinine of 1.15 mg/dl (0.60–1.10 mg/dl), and lactate dehydrogenase of 315 U/l (125–225 U/l). Other data were within normal limits, including beta-D glucan of < 6.0 pg/ ml (< 11.0 pg/ml) and circulating antibodies to HIV of 0.1 S/CO (< 1.0 S/CO). Intravenous piperacillin 2 g × 2/day was initiated for 1 week as an empirical treatment for bacterial cellulitis. Pairs of blood cultures were negative. One week later, intravenous merope-nem at 0.5 g × 2/day was administered. However, no improvement in the cellulitis of the left arm was perceived. Finally, histopathological observations of a skin biopsy specimen from the cellulitis with haematoxylin-eosin stain, Grocott stain and periodic acid-Schiff stain revealed yeast-like microbes 2 weeks after the administration of antibiotics. …
منابع مشابه
Localized genital bullous pemphigoid; A case report
Bullous pemphigoid (BP) is an autoimmune bullous disorder with urticarial pruritic papules and plaques and tense bullae in flexural surfaces of body. The localized form of the disease is a rare variant which can be triggered by different stimuli. Hereunder, we report a patient with the local type involving genitalia without any triggering factors.
متن کاملBullous Pemphigoid: A descriptive study on patients admitted in Loghman Hakim Hospital in Tehran in 1992-97
Background: Most of patients with bullous pemphigoid are at old age and its differentiation from other bullous diseases is important. There is no report of it in Iran. Objective: This study was done in order to determine clinical and paraclinical features, natural course and response to treatment in patients with bullous pemphigoid admitted in Loghman Hakim Hospital in 1992-1997. Patients and M...
متن کاملAssociation between HLA-DQB1*03:01 and Bullous Pemphigoid in Iranian Patients
Background: A common Human Leukocyte Antigen (HLA) class II allele, DQβ1*03:01, seems to be associated with Bullous pemphigoid (BP) in Caucasians whereas previous studies in other ethnic groups showed other HLA class II alleles as genetic predisposing factors for BP. Objective: To investigate the association of HLA class II alleles and haplotypes with BP in Iranian population. Methods: Fifty pa...
متن کاملSerum protein carbonyl and total antioxidant capacity levels in pemphigus vulgaris and bullous pemphigoid
Background: Pemphigus diseases including pemphigus vulgaris (PV) and bullous pemphigoid (BP) are autoimmune diseases that cause severe blistering of the skin and mucous membranes. Among inflammatory mediators, reactive oxygen species (ROS) are involved in the pathogenesis of a wide variety of diseases through oxidative stress for which protein carbonyl (PC) and total antioxidant capacity (TAC) ...
متن کاملEvaluation of direct immunofluorescense on salt split skin in the differentiation of subepidermal autoimmune Bullous dermatoses
Background: Bullous pemphigoid (BP) is the prototype of subepidermal autoimmune bullous dermatoses (SABDs). Direct immunofluorescence on salt split skin substrate (DIF-SS) is one of the methods used to differentiate this group of dermatoses. Objective: We conducted this study in order to delineate the results of DIF-SS in SABD patients. Patients and Methods: Seventeen patients with a BP-like cl...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Acta dermato-venereologica
دوره 93 2 شماره
صفحات -
تاریخ انتشار 2013