Author(s): Molly D’Souza (Nives UMI)

Email(s): nivesdsouza25@gmail.com

DOI: 10.5958/2454-2652.2018.00004.5   

Address: Molly D’Souza (Sr. Nives UMI)
Associate Professor, Holy Family Institute of Nursing Education, Premier Road, Kurla West, Mumbai-400070.
*Corresponding Author

Published In:   Volume - 6,      Issue - 1,     Year - 2018


ABSTRACT:
Granulomatosis with polyangiitis (GPA), formerly known as Wegener granulomatosis, is a rare multisystem autoimmune disease of unknown etiology. Its hallmark features include necrotizing granulomatous inflammation and pauci-immune vasculitis in small- and medium-sized blood vessels. Granulomatosis with polyangiitis (GPA) is a serious disease and without treatment can be fatal within months. Management is directed toward stopping the inflammation process by suppressing the immune system.1 Granulomatosis with polyangiitis poses a significant diagnostic dilemma due its diverse presentations. Seemly isolated sites of disease, such as oral ulcers, may present to physicians working in primary care settings, the emergency room, and subspecialty fields as well as to dentists. Oral presentations are particularly challenging to identify and require a high index of suspicion and a detailed knowledge of the condition in order to diagnose and treat.3


Cite this article:
Molly D’Souza (Nives UMI). WAGNER’S Granulomatosis. Int. J. of Advances in Nur. Management. 2018; 6(1): 15-18. doi: 10.5958/2454-2652.2018.00004.5


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DOI: 10.5958/2454-2652 

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