Acquired idiopathic generalized anhidrosis
Indian Journal of Dermatology, 2015 Acquired idiopathic generalized anhidrosis is a rare condition, where the exact pathomechanism is unknown. We report a case of acquired idiopathic generalized anhidrosis in a patient who later developed lichen planus.
Geethu Gangadharan +2 more
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Congenital Insensitivity to Pain With Anhidrosis: First Reported Case in Nepal [PDF]
Clinical Case ReportsCongenital insensitivity to pain with anhidrosis is a rare autosomal recessive disorder characterized by anhidrosis, self‐mutilation, and insensitivity to pain and temperature.
Sobin Pant +4 more
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Ion Channel and Ubiquitin Differential Expression during Erythromycin-Induced Anhidrosis in Foals [PDF]
Animals, 2021 Macrolide drugs are the treatment of choice for Rhodococcus equi infections, despite severe side-effects temporary anhidrosis as a. To better understand the molecular biology leading to macrolide induced anhidrosis, we performed skin biopsies and ...
Laura Patterson Rosa +3 more
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Anesthetic management of a child with congenital insensitivity to pain with anhidrosis: A case report [PDF]
Frontiers in Surgery, 2022 Congenital insensitivity to pain with anhidrosis (CIPA) is a rare, autosomal recessive disease classified as hereditary sensory and autonomic neuropathy type VI. Patients with CIPA are characterized by insensitivity to pain, episodes of unexplained fever,
Ying Zhang, Zhiyu Geng
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Idiopathic Acquired Anhidrosis: Reversible Generalized Anhidrosis after Sunstroke
The Journal of Dermatology, 1999 AbstractIdiopathic acquired generalized anhidrosis is a very rare condition in which the pathogenesis is still unknown. Although varied findings have been reported, no consistent abnormal findings in sweat glands have been established by histological study or electronmicroscopic study.
T S, Chung, S H, Lee
openaire +5 more sources
Erythroderma, Alopecia, Anhidrosis, and Vitiligo as Complications of a Red Ink Tattoo—A Case Report [PDF]
Clinics and PracticeBackground: Adverse reactions to tattoo pigments are increasingly recognized, yet severe systemic complications remain rare and poorly characterized. Red tattoo ink, in particular, is associated with delayed hypersensitivity reactions, but widespread ...
Mateusz K. Mateuszczyk +4 more
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Anesthetic management of a patient with congenital insensitivity to pain with anhidrosis by coadministration of remifentanil [PDF]
JA Clinical Reports, 2018 Background Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disease characterized by unexplained fever, systemic insensitivity to pain, anhidrosis, and mental distress.
Yoko Takeuchi +5 more
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An allergic subtype of acquired idiopathic generalized anhidrosis resistant to steroid pulse therapy – a retrospective, single-center, cohort study [PDF]
Journal of Cutaneous Immunology and AllergySteroid pulse therapy is considered effective in the treatment of acquired idiopathic generalized anhidrosis (AIGA). However, nearly half of patients with AIGA do not respond to treatment, or relapse, suggesting the need to stratify patients on the basis
Maiko Fujita +8 more
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Ross syndrome following COVID-19 infection in an 18-year-old Syrian male patient: a case report [PDF]
Journal of Medical Case ReportsBackground Ross syndrome is an exceptionally rare disorder characterized by tonic pupils, areflexia, and anhidrosis, with a prevalence that appears to be higher in women than in men, typically presenting in individuals during their 30s.
Ahed Assaf +5 more
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Asymmetric anhidrosis in MSA [PDF]
Neurology, 2003 Thermodysregulation with loss of sweating is a common feature of dysautonomia in multiple system atrophy (MSA).1,2⇓ A 51-year-old man with MSA with …
C, Saft +4 more
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