Familial epidermolysis bullosa simplex– A case report

Authors

  • Neerja Puri PUNJAB HEALTH SYSTEMS CORPORATION PUNJAB (INDIA)

DOI:

https://doi.org/10.66344/jpad.v32i3.1961

Abstract

Epidermolysis bullosa is a rare disorder with frequent blistering at trauma prone sites. We report a case of 10 days old female infant presenting with flaccid yellow colored fluid filled blisters over the extremities. On histopathological examination, a diagnosis of epidermolysis simplex was made. After treatment with appropriate antibiotic, the infant was discharged in satisfactory condition. The treatment options include optimal wound care and prevention of trauma. Newer therapies like gene therapy are in the pipeline, but still have a long way to go before some specific treatment can be advocated.  

Author Biography

  • Neerja Puri, PUNJAB HEALTH SYSTEMS CORPORATION PUNJAB (INDIA)

    CONSULTANT DERMATOLOGIST

References

1. Pearson RW. Studies on the pathogenesis of epidermolysis bullosa. J Invest Dermatol. 1962;39:551-75.

2. Fine JD, Eady RA, Bauer EA, Bauer JW, Bruckner-Tuderman L, Heagerty A, et al. The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus meeting on Diagnosis and Classification of EB. J Am Acad Dermatol. 2008;58:931-50.

3. Intong LRA, Murrell DF. Inherited epidermolysis bullosa: New diagnostic criteria and classification. Clin Dermatol. 2012;30:70-7.

4. Fine JD, Burge SM. Genetic blistering diseases. In: Burns DA, Breathnach S, Cox N, Griffiths C, editors. Rook's textbook of dermatology. 7 th ed. Oxford: Wiley Blackwell; 2010. p. 39.1-39.37.

5. Intong LRA, Murrell DF. How to take skin biopsies for epidermolysis bullosa. Dermatol Clin. 2010;28:197-200.

6. Cepeda-Valdes R, Pohla-Gubo G, Borbolla-Escoboza JR, Barboza-Quintana O, Ancer-Rodriguez J, Hintner H, et al. Immunofluorescence mapping for diagnosis of congenital epidermolysis bullosa. Actas Dermosifiliogr. 2010;101:673-82.

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Published

27.08.2022

Issue

Section

Case Reports

How to Cite

1.
Familial epidermolysis bullosa simplex– A case report. J Pak Assoc Dermatol [Internet]. 2022 Aug. 27 [cited 2026 Sep. 14];32(3):635-7. Available from: https://www.jpad.com.pk/index.php/jpad/article/view/1961