Dystrophic Epidermolysis Bullosa (DEB): How Can Pregnancy Alter the Course of This Rare Disease? An Updated Literature Review on Obstetrical Management with an Additional Italian Experience

Author:

Vimercati Antonella1ORCID,Cazzato Gerardo2,Lospalluti Lucia3,Foligno Stefania3,Taliento Cristina4,Trojanowska Katarzyna Beata5,Cicinelli Ettore1,Bonamonte Domenico3,Caliandro Dario6,Vitagliano Amerigo1,Nicolì Pierpaolo1ORCID

Affiliation:

1. Unit of Obstetrics and Gynecology, Department of Interdisciplinary Medicine (DIM), University of Bari “Aldo Moro”, Policlinico of Bari, Piazza Giulio Cesare 11, 70124 Bari, Italy

2. Department of Emergency and Organ Transplantation (DETO), Section of Pathology, University of Bari “Aldo Moro”, Policlinico of Bari, Piazza Giulio Cesare 11, 70124 Bari, Italy

3. Department of Biomedical Sciences and Human Oncology (DIMO), Section of Dermatology and Venereology, University of Bari “Aldo Moro”, Policlinico of Bari, Piazza Giulio Cesare 11, 70124 Bari, Italy

4. Department of Medical Sciences, Obstetrics and Gynecology Unit, University Hospital “Sant’Anna”, 44121 Ferrara, Italy

5. Section II of Anesthesia and Resuscitation, Policlinico of Bari, 70121 Bari, Italy

6. Pelvic Floor Center, Department of Gynaecology and Obstetrics, Pia Fondazione “Card. G. Panico”, 73039 Tricase, Italy

Abstract

Epidermolysis Bullosa (EB) is an extremely rare and disabling inherited genetic skin disease with a predisposition to develop bullous lesions on the skin and inner mucous membranes, occurring after mild friction or trauma, or even spontaneously. Within the spectrum of EB forms, dystrophic EB (DEB) represents the most intriguing and challenging in terms of clinical management, especially with regard to pregnancy, due to the highly disabling and life-threatening phenotype. Disappointingly, in the literature little focus has been directed towards pregnancy and childbirth in DEB patients, resulting in a lack of sound evidence and guidance for patients themselves and clinicians. The current study aims to contribute to the DEB literature with an updated summary of the existing evidence regarding the obstetrical and anesthesiological management of this rare disease. Furthermore, this literature review sought to answer the question of whether, and if so, in which way, the pregnancy condition may alter the course of the underlying dermatologic skin disease. Having all this information is indispensable when counseling a patient with DEB who desires a child or is expecting one. Finally, we reported own experience with a pregnant woman with a recessive DEB whom we recently managed, with a favorable outcome.

Publisher

MDPI AG

Reference36 articles.

1. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility;Has;Br. J. Dermatol.,2020

2. (2024, April 15). Available online: https://www.osservatoriomalattierare.it/malattie-rare/epidermolisi-bollosa.

3. Overview of epidermolysis bullosa;Sawamura;J. Dermatol.,2010

4. Epidemiology of Inherited Epidermolysis Bullosa Based on Incidence and Prevalence Estimates From the National Epidermolysis Bullosa Registry;Fine;JAMA Dermatol.,2016

5. A study on the estimation of prevalence of epidermolysis bullosa in Japan;Inaba;Nihon Hifuka Gakkai Zasshi,1989

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