TY - JOUR
T1 - Hydroa vacciniforme-like eruptions in a patient with chronic active EB virus infection
AU - Katagiri, Yoshiyuki
AU - Mitsuhashi, Yoshihiko
AU - Kondo, Shigeo
AU - Kanazawa, Chikako
AU - Iwatsuki, Keiji
AU - Tsunoda, Takahiko
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2003/5/1
Y1 - 2003/5/1
N2 - We report a case of chronic active Epstein-Barr (EB) virus infection (CAEBV) associated with skin eruptions mimicking hydroa vacciniforme (HV) in a 4-year-old boy. The patient had repeated episodes of vesiculo-necrotic eruptions on the face, scalp, and bilateral forearms one year before the first visit to our department. General symptoms including fever, hepatosplenomegaly, abnormal liver function, and cervical lymph node swelling were noted three months before the first visit. At the first visit, small, bean-sized, erythemic papules with central necrosis were observed on the face and anterior chest wall. Thumbsized ulcers with crust were present on the bilateral forearms. Histopathological examination of an erythematous lesion in the submandibular area revealed parakeratosis with a thick crust, mild spongiosis in the epidermis, and a dense infiltration of lymphoid cells into the dermis and perivascular space. Laboratory examination showed EBNA x40, EBV VCA IgG x 1,280, and EBV DNA (PCR) 8 × 104. EBV-encoded small nuclear RNA (EBER) positive cells were detected in the dermis by an in situ hybridization (ISH) method. Large granular lymphocytes (65%) with the NK cell phenotype were found in the peripheral blood. A real time PCR method showed 171,741 copies/μg DNA in CD 16 positive cells. Although latent EBV infection-associated eruptions have been documented, detailed skin manifestations in CAEBV are less well known.
AB - We report a case of chronic active Epstein-Barr (EB) virus infection (CAEBV) associated with skin eruptions mimicking hydroa vacciniforme (HV) in a 4-year-old boy. The patient had repeated episodes of vesiculo-necrotic eruptions on the face, scalp, and bilateral forearms one year before the first visit to our department. General symptoms including fever, hepatosplenomegaly, abnormal liver function, and cervical lymph node swelling were noted three months before the first visit. At the first visit, small, bean-sized, erythemic papules with central necrosis were observed on the face and anterior chest wall. Thumbsized ulcers with crust were present on the bilateral forearms. Histopathological examination of an erythematous lesion in the submandibular area revealed parakeratosis with a thick crust, mild spongiosis in the epidermis, and a dense infiltration of lymphoid cells into the dermis and perivascular space. Laboratory examination showed EBNA x40, EBV VCA IgG x 1,280, and EBV DNA (PCR) 8 × 104. EBV-encoded small nuclear RNA (EBER) positive cells were detected in the dermis by an in situ hybridization (ISH) method. Large granular lymphocytes (65%) with the NK cell phenotype were found in the peripheral blood. A real time PCR method showed 171,741 copies/μg DNA in CD 16 positive cells. Although latent EBV infection-associated eruptions have been documented, detailed skin manifestations in CAEBV are less well known.
KW - CAEBV
KW - Chronic active EB virus infection
KW - EB virus
KW - Epstein-Barr
KW - Hydroa vacciniforme
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U2 - 10.1111/j.1346-8138.2003.tb00406.x
DO - 10.1111/j.1346-8138.2003.tb00406.x
M3 - Article
C2 - 12773806
AN - SCOPUS:0038321287
SN - 0385-2407
VL - 30
SP - 400
EP - 404
JO - Journal of Dermatology
JF - Journal of Dermatology
IS - 5
ER -