A case report on the management of pemphigus vulgaris along with comorbid conditions in geriatric patient

Pemphigus vulgaris (PV) is a rare autoimmune blistering disease characterized by intraepidermal acantholysis, which affects the skin and mucous membranes. The patient was a 65-year-old female presenting with a history of type 2 diabetes mellitus and hypertension. There were fluid-filled, pruritic lesions that progressively spread from the forearms and neck to the face and other areas. Histopathological and immunofluorescence studies confirmed PV. She was treated with intravenous hydrocortisone, antibiotics, antihistamines, and supportive measures. The basic chronic kidney disease needed to be considered, and thus, conservative treatment was opted for. On being discharged, she was given a tapering dose of prednisolone along with other drugs that were prescribed for antidiabetic and antihypertensive drugs. It is a case that emphasizes the early and multidisciplinary need for diagnosis in PV, especially when comorbidities are present. Further research is also sought to improve the procedures of diagnosis and treatment of PV.

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Publication Details

Journal
Global Journal of Health Sciences and Research
Published
2024-11-19
DOI
https://doi.org/10.25259/gjhsr_45_2024
Primary Topic
Autoimmune Bullous Skin Diseases
Type
article
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article

A case report on the management of pemphigus vulgaris along with comorbid conditions in geriatric patient

Swetha Chandru, S. Prashanth, G. Nithish, R. Ponraja
Global Journal of Health Sciences and Research
Autoimmune Bullous Skin Diseases
article

A case report on the management of pemphigus vulgaris along with comorbid conditions in geriatric patient

Swetha Chandru, S. Prashanth, G. Nithish, R. Ponraja
article en

Abstract

Pemphigus vulgaris (PV) is a rare autoimmune blistering disease characterized by intraepidermal acantholysis, which affects the skin and mucous membranes. The patient was a 65-year-old female presenting with a history of type 2 diabetes mellitus and hypertension. There were fluid-filled, pruritic lesions that progressively spread from the forearms and neck to the face and other areas. Histopathological and immunofluorescence studies confirmed PV. She was treated with intravenous hydrocortisone, antibiotics, antihistamines, and supportive measures. The basic chronic kidney disease needed to be considered, and thus, conservative treatment was opted for. On being discharged, she was given a tapering dose of prednisolone along with other drugs that were prescribed for antidiabetic and antihypertensive drugs. It is a case that emphasizes the early and multidisciplinary need for diagnosis in PV, especially when comorbidities are present. Further research is also sought to improve the procedures of diagnosis and treatment of PV.

Global Journal of Health Sciences and ResearchVol. 0
Goverment Siddha Medical College (IN)
Good health and well-being
Openalex Percentile: Top 67%
Autoimmune Bullous Skin Diseases
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