![]() About the Disease Diagnosis & Treatment Living with the Disease Research Diagnostic Process Building a Medical Team Getting a Diagnosis Navigate to sub-section. NSV can come about at any age (unlike segmental vitiligo, which is far more prevalent in teenage years). Alopecia universalis, onychodystrophy, and total vitiligo Alopecia universalis, onychodystrophy, and total vitiligo. Repigmentation in Vitiligo Universalis After Starting Anti-tubercular. Patients with vitiligo exhibit depigmented patches on the skin that are extremely sensitive for sunburns and that may impair cosmetic appearance and. This case provides an important reminder for physicians to monitor such severe complications after DIHS. Extreme cases of vitiligo, to the extent that little pigmented skin remains, are referred to as vitiligo universalis. The Global Vitiligo Foundation president and the meeting chairs will welcome. ![]() The occurrence of widespread vitiligo after DIHS is an extremely rare condition. Acrofacial type 4 cases each (10) & universalis was seen only in 2 cases (5). Further immunoserology study showed elevated plasma C-X-C motif chemokine 10 level, which is related to vitiligo activity, in our patient. An observational study of Vitiligo - By Krishnendra Varma, Ujjwal Kumar. Some spontaneous repigmentation was noted 4 years after DIHS without specific treatment. Histopathological examination confirmed the diagnosis of vitiligo. Generalized hypopigmentation of the skin and leukotrichia were noted 4 months after the onset of DIHS. Reactivation of human herpesvirus 6 and possible reactivation of cytomegalovirus were detected. ![]() therapy in vitiligo universalis with topical 4-methoxyphe. The patient was treated with immunosuppressants including systemic corticosteroid for approximately 1.5 years due to recurrent episodes. Vitiligo is a depigmenting disorder characterized by the progressive loss of melanocytes. The patient was diagnosed with definite DIHS. We report a 47-year-old woman who presented with fever, generalized maculopapular eruption, facial edema and eosinophilia with liver function impairment after taking celecoxib and sulfasalazine for 1 month. DIHS patients have been reported to subsequently develop autoimmune disease, which may be followed by end-organ decompensation. Drug-induced hypersensitivity syndrome (DIHS) is a type of severe drug adverse reaction with high morbidity and mortality.
0 Comments
Leave a Reply. |