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A rare serpiginous pattern of epidermolysis bullosa pruriginosa
Corresponding author: Dr. Priyanka Patil, Department of Dermatology, Dr D.Y. Patil Medical College, Hospital and Research Centre, Pimpri, Pune, Maharashtra, India. priyanka.patil1221997@gmail.com
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Received: ,
Accepted: ,
How to cite this article: Raman T, Patil P, Asnani DR. A rare serpiginous pattern of epidermolysis bullosa pruriginosa. Indian J Dermatol Venereol Leprol. doi: 10.25259/IJDVL_584_2024
A 31-year-old man presented with a history of symmetrical, extremely pruritic, raised skin lesions associated with oozing of clear fluid over the lower limbs and back for 20 years. The patient mentioned the presence of preceding fluid-filled lesions and was distressed by the appearance which severely hampered his quality of life.
On examination, multiple linear hyperpigmented, lichenified plaques with atrophic scarring in a serpiginous pattern were seen over bilateral lower limbs and sacral area. A few tense bullae were present over the shins with multiple, well-defined hypopigmented patches over the lower limbs and back, indicating previous lesions. [Figure 1]
Histopathology revealed hyperkeratosis with focal parakeratosis. Epidermis showed a suprabasal bullous lesion with RBCs, fibrin, and scanty neutrophils. Dermis revealed a mild increase in collagen bundles, focal melanin incontinence, and perivascular mild chronic inflammatory cells. Diagnosis of epidermolysis bullosa pruriginosa was made and symptomatic treatment was given in the form of antihistamines and topical steroids.
A linear pattern of lesions has been reported, serpiginous pattern as seen in our case is quite rare.
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Conflicts of interest
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