Das klinische und histologische Bild der Acrodermatitis continua

Kogoj, F

doi:10.1007/bf00362041

Cited by 19 publications

(2 citation statements)

References 5 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Individual variations in the extent of transgressive pachyderma are well documented in the literature, and widespread involvement up to the antecubital fossae and above the ankles ("socks and gloves") has been reported (9,15,16). We also observed individual variations in the extent of involved skin.…”

Section: Discussionmentioning

confidence: 97%

Mal de Meleda: A Report of Four Cases from the United Arab Emirates

Lestringant

Frossard

Adeghate

et al. 1997

Pediatric Dermatology

View full text Add to dashboard Cite

Mal de Meleda (MDM), or recessive transgressive palmoplantar keratoderma, is a rare disorder. MDM may have originated as a founder mutation that occurred on the island of Meleda, now Mljet, in Croatia, where it was first described. However, the condition has also been observed in countries distant from Mljet. The presentation of the disease in young patients has not been reported and the progressiveness of the lesions is debated. We examined four young United Arab Emirates nationals patients (ages 7 months to 12 years) who presented with keratoderma palmoplantaris (KPP) and transgressive pachyderma (TP) that had both been present before 1 year of age. KPP and TP were more pronounced in the two oldest patients. Family histories were consistent with autosomal recessive inheritance. The development of MDM lesions appears to be age-related. However, environment and individual factors may also play a role in the development and persistence of the lesions. Molecular genetic studies are necessary to establish whether the broad clinical presentation of the disease is due to allelic or genetic heterogeneities.

show abstract

Section: Discussionmentioning

confidence: 97%

Mal de Meleda: A Report of Four Cases from the United Arab Emirates

Lestringant

Frossard

Adeghate

et al. 1997

Pediatric Dermatology

View full text Add to dashboard Cite

show abstract

“…However, these authors also believed that the disease was indistinguishable from pustular psoriasis on histopathology. Over the years, many studies 17–19 have attempted to assess the relationship of ACH with psoriasis. Hence, it has been concluded that ACH is a variant of pustular psoriasis.…”

Section: Introductionmentioning

confidence: 99%

Acrodermatitis continua of Hallopeau: evolution of treatment options

Sehgal¹,

Verma²,

Sharma

et al. 2011

Int J Dermatology

117

View full text Add to dashboard Cite

Ever since its inception, acrodermatitis continua of Hallopeau, has been recognized as an uncommon clinical entity which has been sparingly reported from across the globe. The attempt to have cumulative information on prevalent nomenclature, definition, reminiscences, and clinical overtures has brought differential diagnosis and diagnosis in sharp focus, the highlights of which are outlined. Hence, it was considered important to review the evolution of treatment options available thus far including use of biologics.

show abstract

Franjo Kogoj (1894–1983)

Rupec¹,

Dobrić²

2008

Pantheon Der Dermatologie

View full text Add to dashboard Cite

Das klinische und histologische Bild der Acrodermatitis continua

Cited by 19 publications

References 5 publications

Mal de Meleda: A Report of Four Cases from the United Arab Emirates

Mal de Meleda: A Report of Four Cases from the United Arab Emirates

Acrodermatitis continua of Hallopeau: evolution of treatment options

Franjo Kogoj (1894–1983)

Contact Info

Product

Resources

About