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Infantile Eosinophilic Pustular Folliculitis: A Case Report
Journal of Cosmetic Dermatology 2022 Cilt 21 Sayı 3
Scopus Eşleşmesi Bulundu
5
Atıf
21
Cilt
1143-1146
Sayfa
Özet
Background: Infantile eosinophilic pustular folliculitis (I-EPF) is a rare disease characterized by pruritic vesicles and sterile pustules on the erythematous surface of the scalp and facial localization, usually seen in the neonatal period. It is essential to show the presence of dense eosinophils in the diagnosis of pustules. Histopathological examination of the hair follicles by eosinophils infiltration is determined. Aim: Here, we reported a 5-month-old baby boy diagnosed infantile eosinophilic pustular folliculitis. Patient: A 5-month-old baby boy was consulted to our polyclinic by his family because of pustules on the scalp, face, and neck developing in two week after birth. In dermatological examination, the pustular lesions of 1-2 mm in diameter on the scalp, face, and neck on an erythematous background were determined. Results: There was no growth in the culture taken from the pustule. In the laboratory tests of the patient; upon detection of eosinophilia in the hemogram. The eosinophil count at the patient's first admission was 1.48 K/μl. (0.05 0.50). Eosinophil count was 0.02 K/μl after treatment. It was decreased. The patient was evaluated for other pustular dermatoses. In the differential diagnosis of the patient; causing bacterial/non-bacterial pustulosis were included. Bacterial culture was negative. Conclusion: Eosinophilic folliculitis defines as a group of papulopustular diseases with unknown etiology characterized histologically by eosinophilic infiltrates. First, Ofuji reported a female patient with recurrent follicular pustules and peripheral eosinophilia as a variant of folliculitis in 1965. Its etiopathogenesis is not clearly known. In the differential diagnosis of EPF includes the other pustular lesions of the newborn such as erythematoxicum neonatarum, transient neonatal pustular dermatosis, infantile acropustulosis, scabies, dermatophytosis, and langerhans cell histiocytosis. Treatment options includes topical corticosteroids and calcineurin inhibitors, antihistamines, systemic antibacterial and anti-inflammatory agents, and dapson.
Web of Science Eşleşmesi Bulundu
5
WoS Atıf
21
Cilt
Article
Belge Türü
Kaynak: JOURNAL OF COSMETIC DERMATOLOGY · s. 1143-1146
Anahtar Kelimeler (WoS)

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Scimago Dergi Bilgisi Otomatik ISSN Eşleştirmesi 2022 yılı verileri
Journal of Cosmetic Dermatology
Q2
SJR Quartile
0,610
SJR Skoru
67
H-Index
Kategoriler: Dermatology (Q2)
Alanlar: Medicine
Ülke: United Kingdom · John Wiley and Sons Inc
Bu bilgiler makale yılına göre Scimago veritabanından ISSN eşleştirmesiyle otomatik getirilmektedir. Dergi sıralama verileri Scimago'nun ilgili yılı baz alınmaktadır.

Anahtar Kelimeler

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Makale Bilgileri

Dergi Journal of Cosmetic Dermatology
ISSN 1473-2165
Yıl 2022 / 3. ay
Cilt / Sayı 21 / 3
Sayfalar 1143 – 1146
Makale Türü Vaka Takdimi
Hakemlik Hakemli
Endeks SCI-Expanded
JCR Quartile Q3
Teşvik Puanı 1,44 · YÖKSİS Akademik Teşvik
Yayın Dili İngilizce
Kapsam Uluslararası
Toplam Yazar 5 kişi
Erişim Türü Elektronik
Alan Sağlık Bilimleri Temel Alanı Deri ve Zührevi Hastalıkları

YÖKSİS Yazar Kaydı

Yazar Adı SAYLAM KURTİPEK GÜLCAN, ZEKEY EMRE, TUNÇEZ AKYÜREK FATMA, DEMİRBAŞ ABDULLAH, HARMANKAYA İSMAİL
YÖKSİS ID 5692816

Metrikler

Scopus Atıf 5
Havuz Atıfları 0
JCR Quartile Q3
Teşvik Puanı 1,44
Yazar Sayısı 5