1.The Koebner Phenomenon in Erythema Multiforme after Getting Acupuncture and Cupping Glass Therapy.
Eun Joo JANG ; Dong Yoon LEE ; Ji Yeoun LEE ; Mi Kyeong KIM ; Tae Young YOON
Korean Journal of Dermatology 2011;49(9):809-811
Since its first description in 1887 as the appearance of psoriatic lesions in the uninvolved skin of psoriatic patients as a consequence of trauma, the Koebner phenomenon has been described in numerous diseases. Several types of injury can trigger the Koebner phenomenon, such as physical injury, surgical wound, irritation, sunburn, or radiation therapy. In this report, we describe a 43-year-old woman who developed erythema multiforme which was accompanied by the Koebner phenomenon after getting acupuncture and cupping glass therapy. The purpose of the report is to broaden our awareness of the spectrum of injury that can trigger the Koebner phenomenon.
Acupuncture
;
Adult
;
Erythema
;
Erythema Multiforme
;
Female
;
Glass
;
Humans
;
Intraoperative Complications
;
Skin
;
Sunburn
2.Leprosy presented as cutaneous erythema.
Fang WANG ; Sonia Kay HWANG ; Hai-yan HUANG ; Juan DU ; Xiao-lan DING ; Soe Lwin MYINT ; Jian-zhong ZHANG
Chinese Medical Journal 2013;126(19):3797-3797
4.A woman with erythematous plaques.
Sai Yee CHUAH ; Yen Loo LIM ; Joyce S S LEE ; Hiok Hee TAN
Annals of the Academy of Medicine, Singapore 2013;42(8):419-421
5.Antiphospholipid syndrome.
Chinese Journal of Pediatrics 2003;41(2):154-157
Abortion, Habitual
;
complications
;
Antibodies, Antiphospholipid
;
blood
;
Antiphospholipid Syndrome
;
complications
;
pathology
;
therapy
;
Erythema
;
complications
;
Heart Valve Diseases
;
complications
;
Humans
;
Kidney Diseases
;
complications
;
Skin Diseases
;
complications
;
Thrombosis
;
complications
6.Clinical constellation of annular erythema associated with anti-Ro/La autoantibodies.
Journal of Korean Medical Science 2000;15(2):199-202
Annular erythema (AE) associated with anti-Ro (SSA) and/or La (SSB) autoantibody in patients with Sjogren syndrome (SS) or with SS/systemic lupus erythematosus overlap syndrome (SS/SLE), has recently been described in Orientals, and it may be a counterpart of annular skin lesion of the subacute cutaneous LE seen mostly in Caucasians. The author examined five Korean AE patients in respect to dinical diversity. In this small-sample study, subtle differences appeared between individual cases regarding the serologic features and the diagnoses of the disease. Among the five cases, four had circulating anti-Ro and anti-La antibodies, and one had only anti-La. Regarding the diagnosis, one was SS/SLE, two were primary SS, and the remaining two were only "AE associated with anti-Ro/La antibody". There seem to be a wide clinical spectrum in the disease expression of AE associated with anti-Ro/La autoantibody than previously thought.
Adolescence
;
Adult
;
Antibodies, Antinuclear/immunology*
;
Case Report
;
Erythema/immunology*
;
Erythema/etiology
;
Female
;
Human
;
Lupus Erythematosus, Systemic/immunology*
;
Lupus Erythematosus, Systemic/complications
;
Male
;
Sjogren's Syndrome/immunology*
;
Sjogren's Syndrome/complications
7.Two Cases of Pruritic Urticarial Papules and Plaques of Pregnancy in the Postpartum.
Jiwon BYUN ; Bo Hee YANG ; Sung Hyub HAN ; Hee Jin SONG ; Hyeon Sook LEE ; Gwang Seong CHOI ; Jeonghyun SHIN
Korean Journal of Dermatology 2010;48(3):228-231
Pruritic urticarial papules and plaques of pregnancy (PUPPP), also known as a polymorphic eruption of pregnancy, is the most common dermatosis of pregnancy. Typically, PUPPP starts with erythema and urticarial papular eruption in the abdominal striae and may extend to the buttocks and thighs. It usually evolves in the third trimester and resolves rapidly in the postpartum. It is not usually recurrent in subsequent pregnancies. We report herein two patients with postpartum PUPPP.
Buttocks
;
Erythema
;
Female
;
Humans
;
Postpartum Period
;
Pregnancy
;
Pregnancy Complications
;
Pregnancy Trimester, Third
;
Pruritus
;
Skin Diseases
;
Thigh
8.Hypereosinophilic syndrome in a 2 month-old infant.
Xiao-ran AN ; Xing-guo WANG ; Jing-hua CHEN ; Xiao-feng YUAN ; Li CONG ; Ji-fang WANG ; Guang-shen LI
Chinese Journal of Pediatrics 2003;41(5):378-378
Anemia
;
etiology
;
Erythema
;
etiology
;
Fatal Outcome
;
Female
;
Fever
;
etiology
;
Humans
;
Hypereosinophilic Syndrome
;
complications
;
diagnosis
;
Infant
9.Association of human parvovirus B19 infection and childhood idiopathic thrombocytopenic purpura: a meta analysis of Chinese literatures.
Yao-Dong ZHANG ; Qun HU ; Shuang-You LIU ; Ai-Guo LIU ; Guan-Ling WANG ; Hao XIONG ; Yan SUN
Chinese Journal of Contemporary Pediatrics 2009;11(12):999-1001
OBJECTIVETo study the relationship between human parvovirus B19 infection and childhood idiopathic thrombocytopenic purpura (ITP) by the principle of evidence based medicine.
METHODSPapers related to the relationship between human parvovirus B19 infection and childhood ITP published between 1994 and 2008 were retrieved electronically from the Chinese Journals Full-text Database and the Wanfang Data. These relevant papers on case-control trials were statistically studied by meta analysis.
RESULTSEight papers that met the inclusion criteria were included for this meta analysis. Five hundred and sixteen cases of childhood ITP and 246 healthy controls were enrolled. The meta analysis showed that the incidence of human parvovirus B19 infection in the ITP group was significantly higher than that in the control group (OR=13.71, 95% CI=7.07-26.59, Z=7.75, p<0.01).
CONCLUSIONSHuman parvovirus B19 infection is closely associated with childhood ITP.
Child ; Erythema Infectiosum ; complications ; Female ; Humans ; Male ; Purpura, Thrombocytopenic, Idiopathic ; etiology
10.Hemophagocytic Syndrome Secondary to Human Parvovirus B19 Infection in an Acquired Immunodeficiency Syndrome Patient:Report of One Case.
Yan ZHANG ; Jun YAN ; Fei WANG ; Jin GAO ; Kai-Long GU ; Ai-Fang XU
Acta Academiae Medicinae Sinicae 2023;45(3):530-532
The acquired immunodeficiency syndrome patients with compromised immunity are prone to hemophagocytic syndrome secondary to opportunistic infections.This paper reports a rare case of hemophagocytic syndrome secondary to human parvovirus B19 infection in an acquired immunodeficiency syndrome patient,and analyzes the clinical characteristics,aiming to improve the diagnosis and treatment of the disease and prevent missed diagnosis and misdiagnosis.
Humans
;
Lymphohistiocytosis, Hemophagocytic/drug therapy*
;
Erythema Infectiosum/complications*
;
Acquired Immunodeficiency Syndrome/complications*
;
Parvoviridae Infections/diagnosis*
;
Parvovirus B19, Human