TY - JOUR
T1 - Juvenile dermatomyositis in a 6 year old boy
T2 - A rare case
AU - Sunarto, Olivia Awwalin
AU - Rahmadewi,
AU - Wardhani, Putri Hendria
AU - Widia, Yuri
AU - Indranarum, Trisiswati
AU - Citrashanty, Irmadita
AU - Damayanti,
AU - Sawitri, Sawitri
AU - Murtiastutik, Dwi
N1 - Publisher Copyright:
© 2024 Pakistan Association of Dermatologists. All rights reserved.
PY - 2024/10
Y1 - 2024/10
N2 - Juvenile Dermatomyositis (JDM) is a systemic capillary vasculopathy and idiophatic inflammatory myopathies (IIM) in children. It is a rare disease with incidence in the United States 3 per million children per year. A 6-year-old child complained about red spots on his right and left knees. He had red spots which became white spots and thickening skin on his knuckles since 4 months ago before hospitalized. Redness occurred around the eyes and his back since 2 months ago. He had muscle weakness especially on his limb since 2 months ago. JDM has peak occurrence during infancy with ages of 5 and 15. Genetic, environmental and immunological factors are believed to contribute to the development of JDM. The clinical symptoms of this condition are varied, with different levels of skin, muscle, gastrointestinal and cardiac. The goals of treatment are to control inflammatory myositis and prevent complication. It is important for dermatologist to know this disease clearly, so that can make a proper diagnosis and carry out appropriate management.
AB - Juvenile Dermatomyositis (JDM) is a systemic capillary vasculopathy and idiophatic inflammatory myopathies (IIM) in children. It is a rare disease with incidence in the United States 3 per million children per year. A 6-year-old child complained about red spots on his right and left knees. He had red spots which became white spots and thickening skin on his knuckles since 4 months ago before hospitalized. Redness occurred around the eyes and his back since 2 months ago. He had muscle weakness especially on his limb since 2 months ago. JDM has peak occurrence during infancy with ages of 5 and 15. Genetic, environmental and immunological factors are believed to contribute to the development of JDM. The clinical symptoms of this condition are varied, with different levels of skin, muscle, gastrointestinal and cardiac. The goals of treatment are to control inflammatory myositis and prevent complication. It is important for dermatologist to know this disease clearly, so that can make a proper diagnosis and carry out appropriate management.
KW - Juvenile Dermatomyositis
KW - Rare disease
KW - Systemic autoimmune disease
KW - Vasculophaty disease
UR - http://www.scopus.com/inward/record.url?scp=85206836205&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:85206836205
SN - 1560-9014
VL - 34
SP - 1116
EP - 1122
JO - Journal of Pakistan Association of Dermatologists
JF - Journal of Pakistan Association of Dermatologists
IS - 4
ER -