1.Hailey-Hailey Disease Treated with Topical Tacalcitol.
Su Young JEON ; Seung Min HA ; Dong Yeob KO ; Ki Hoon SONG ; Ki Ho KIM
Annals of Dermatology 2013;25(3):389-390
No abstract available.
Dihydroxycholecalciferols
;
Pemphigus, Benign Familial
2.The Effect of Cryotherapy in Hailey-Hailey Disease.
Jee Hee SON ; Yong Se CHO ; Yun Sun BYUN ; Bo Young CHUNG ; Chun Wook PARK ; Hye One KIM
Annals of Dermatology 2017;29(1):117-118
No abstract available.
Cryotherapy*
;
Pemphigus, Benign Familial*
3.A Case of Hailey-Hailey Disease with a Novel Nonsense Mutation in the ATP2C1 Gene.
Hazuki YASUDA ; Nobuo KANAZAWA ; Mitsuhiro MATSUDA ; Takahiro HAMADA ; Minao FURUMURA ; Takashi HASHIMOTO ; Takekuni NAKAMA ; Fukumi FURUKAWA
Annals of Dermatology 2017;29(5):642-644
No abstract available.
Codon, Nonsense*
;
Pemphigus, Benign Familial*
6.Successful Treatment of Hailey-Hailey Disease with Aminolevulinic Acid Photodynamic Therapy.
Xiao Xiao YAN ; Hong Qing TIAN ; Chang Liang WANG ; Bao Qi YANG ; Wei Zhi WU ; Fu Ren ZHANG
Annals of Dermatology 2015;27(2):222-223
No abstract available.
Aminolevulinic Acid*
;
Pemphigus, Benign Familial*
;
Photochemotherapy*
7.Spot the difference: A case of Hailey-Hailey Disease in a 64-year-old Filipino female
Raisa Celine R. Rosete ; Juan Paolo David S. Villena ; Mae N. Ramirez-Quizon
Acta Medica Philippina 2021;55(5):563-568
Hailey-Hailey disease (HHD) is an uncommon acantholytic disorder of the skin. This is a case of a 64-year-old Filipino female with a chronic history of painful and malodorous intertriginous plaques. Histopathologic evaluation showed overlapping features of pemphigus vulgaris and Hailey-Hailey disease. A negative direct immunofluorescence test clinched the diagnosis of Hailey-Hailey disease. The patient was advised regarding preventive measures and treated with topical antibiotics and corticosteroids with improvement of her lesions.
Pemphigus, Benign Familial
;
Fluorescent Antibody Technique, Direct
8.A Case of Isolated Acantholytic Acanthoma.
Hye Jin CHOI ; Seung Seog HAN ; Sung Eun CHANG ; Mi Woo LEE ; Jee Ho CHOI ; Kee Chan MOON ; Jai Kyoung KOH
Korean Journal of Dermatology 2005;43(3):391-393
A solitary acantholytic acanthoma is a benign tumor which presents as a solitary asymptomatic, keratotic papule or nodule. The acantholysis, implied in the term, is the histologic hallmark. It may mimic pemphigus vulgaris, pemphigus vegetans, or Hailey-Hailey disease, but displays no evidence of these disorders. We report a case of isolated acantholytic acanthoma in a 78-year-old man, where the histologic feature is focal acantholytic dyskeratosis.
Acantholysis
;
Acanthoma*
;
Aged
;
Humans
;
Pemphigus
;
Pemphigus, Benign Familial
9.A Case of Acantholytic Acanthoma.
Korean Journal of Dermatology 2002;40(7):838-840
Acantholytic acanthoma is typically an asymptomatic, keratotic papule or nodule. In 1988, Brownstein described a previously unrecognized benign acanthoma, the acantholytic acanthoma. The term acantholytic is used because acantholysis is the outstanding histologic feature in this neoplasm; acanthoma is chosen because the growths are benign tumors of epidermal keratinocytes. On histopathology, these tumors may mimic pemphigus vulgaris, pemphigus vegetans, superficial pemphigus, or Hailey-Hailey disease, but had no evidence of any of these disorders. We report a case of acantholytic acanthoma seen on the inguinal area of a 79-year-old man who had a keratotic nodule on the left inguinal area.
Acantholysis
;
Acanthoma*
;
Aged
;
Humans
;
Keratinocytes
;
Pemphigus
;
Pemphigus, Benign Familial
10.A Case of Generalized Pustular Psoriasis in Infancy.
Choong Sang KIM ; Jagn Kue PARK ; Yoo Shin LEE
Korean Journal of Dermatology 1974;12(4):249-253
A case of familiar benign chronic pemphigus is reported. A 41 years old housewife has recurrent history of developing grouped vesicular eruptions with erythematous erosion on the intertrigenous area since 29 years of her age. The lesions were used to aggrevated in summer and improved in autumn. Familiar history revealed same disease of her grand mother, father, 44 year old elder sister and 39 year old younger sister. All of whom had similar clinical signs and symptoms. Routine physical and Iaboratoryfindings were within normal limits. The histopathological findings, from vesicular eruption of the lateral aspect of neck, showed multilocular suprabasal clefts with acantholsis, villi formation and hyperkeratosis. The lesions were improved hy the local application of corticostcroidoid ointrnent only.
Adult
;
Fathers
;
Humans
;
Mothers
;
Neck
;
Pemphigus, Benign Familial
;
Psoriasis*
;
Siblings