Effectiveness of Debridement Treatment in Neonatorum Epidermolysis Bullosa: A Case Report
نویسندگان
چکیده
Introduction: Epidermolysis Bullosa (EB) is an autosomal genetic disorder that characterized by blistering of the skin and mucosa following mild trauma such as frictional trauma. There no definitive treatment has yet to be developed. The goal surgical debridement achieve a clean wound bed in fastest way, reduce bacterial burden, remove much nonvital tissue, speed up healing process, which will shorten length stay hospital. Case Finding: We have 3 days old newborn with clinical appearance similar second degree burn lesion bullous lesions epidermal damage on her both feet, gluteal, genital regions but without previous history contact thermal consulted patients. General physical examination showed fever vital within normal condition. In perinatal history, baby was delivered caesarean section from 37 years-old G3P2A0 mother preeclampsia comorbid, gestational age, birth weight 3800 grams, 51 cm, APGAR scores were 9 10 1st 5th minute respectively. Our patient looked like 2nd injury blisters epidermolysis Consulted plastic surgeon for further evaluation management. Baby discharged day or after management stable Conclusion: demonstrated greatly effective efficient achieving these aims. Observation did not reveal any sign infection, showing controlled symptoms good process. suggest performing would duration hospitalization. Therefore, it provides low-risk nosocomial infection low-cost
منابع مشابه
Epidermolysis Bullosa Puriginosa: Report of a Case
Epidermolysis Bullosa Puriginosa is a genetic mechanobullous disease characterized by pruritus, lichenified or nodular prurigo-like lesions, occasional trauma-induced blistering, excoriations, milia, nail dystrophy and albopapuloid lesions that appear at birth or later. Scarring and prurigo are most prominent on the shins. Herein, we report a case with a history of blisters since childhood foll...
متن کاملEpidermolysis Bullosa associated with pyloric stenosis: A case report
Epidermolysis bullosa are a group of hereditary skin diseases manifested as blisters on the sites of trauma to the skin. According to the level of blister development, epidermolysis bullosa are divided into the following groups: epidermolysis bullosa simplex, junctional epidermolysis bullosa and dystrophic epidermolysis bullosa. The latter two groups are associated with poorer prognosis and hig...
متن کاملJunctional epidermolysis bullosa: a case report.
Epidermolysis bullosa (EB) is a group of genetically determined disorders characterized by blistering of the skin and mucosae. There are three major forms--simple, junctional and dystrophic--and each has several varieties. The present case report describes a male child with junctional EB. The aim of the report is to present the dietary situation and the dental status of the child, examples of p...
متن کاملPretibial Epidermolysis Bullosa: Report of two cases
Pretibial epidermolysis bullosa is a rare variant of hereditary epidermolysis bullosa characterized by the delayed onset of lesions and their localization. We present two cases, a 35-year-old woman and a 21-year-old man. They clinically had pruritus, nodular prurigo-like or lichenified lesions, violaceous scarring, milia, nail dystrophy and in one case albopapuloid lesions on the trunk. Physica...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: International journal of medical science and clinical research studies
سال: 2022
ISSN: ['2767-8326', '2767-8342']
DOI: https://doi.org/10.47191/ijmscrs/v2-i7-17