Atrophoderma of Pasini and Pierini and systemic scleroderma

Bisaccia, E. P.

doi:10.1001/archderm.118.1.1a

Cited by 8 publications

(4 citation statements)

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“…Third, classical morphea plaques may co‐occur with IAPP in the same patient 4,6,11,15 . Fourth, progression from IAPP to systemic scleroderma was described in one patient 24 . In fact, Miller et al 25 considered that the transition from either IAPP to morphea or vice versa may occur at any time during the course of the disease.…”

Section: Discussionmentioning

confidence: 99%

Atrophoderma of Pasini and Pierini: a clinical and histopathological study

et al. 2008

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Section: Discussionmentioning

confidence: 99%

Atrophoderma of Pasini and Pierini: a clinical and histopathological study

et al. 2008

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“…Lesions of "burn-out" morphea may be atrophic similar to that of IAPP (8) and some histologic similarities such as mild sclerosis and collagen homogenization exist in a few cases (1, 9). There was a case report of a patient with typical IAPP who developed progressive systemic sclerosis (10). However, whether this disorder is an end stage of morphea is unclear.…”

Section: Discussionmentioning

confidence: 99%

Congenital Atrophoderma of Pasini and Pierini

et al. 2006

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Idiopathic atrophoderma of Pasini and Pierini is a form of dermal atrophy of unknown etiology, usually affecting women during their adolescence and young adulthood. A 2-yr-old girl was presented with erythematous atrophic lesion on the right shoulder, which appeared from birth. The histologic findings were consistent with atrophoderma. This patient, to the best of our knowledge, is the first case of atrophoderma with an onset since birth.

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“…In addition, one of our patients also had lichen planus, and changes over her trunk clinically consistent with atrophoderma of Pasini and Pierini. The latter is regarded by some authors as a variant of morphoea and there have been reports of its progression to morphoea or systemic sclerosis 34–36 . However, other authors have regarded it as a distinct condition from morphoea because of dermal atrophy and the typical absence of sclerosis 37 .…”

Section: Discussionmentioning

confidence: 99%

Genital lichen sclerosus associated with morphoea or systemic sclerosis: clinical and HLA characteristics

Farrell¹,

Marren²,

Wojnarowska³

2000

British Journal of Dermatology

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Although patients with both morphoea and lichen sclerosus have been reported previously, in the majority of these reports the lichen sclerosus has been extragenital. We report nine patients in whom genital lichen sclerosus coexisted with scleroderma spectrum disorders including seven with morphoea, one with morphoea and lichen planus, and one with systemic sclerosis. The clinical features, associated autoimmune disease, autoantibodies and HLA type are reported. Antibodies to Borrelia burgdorferi were not detected in any of the patients. The coexistence of these diseases raises a number of intriguing questions about the relationship between them.

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Atrophoderma of Pasini and Pierini and systemic scleroderma

Cited by 8 publications

References 0 publications

Atrophoderma of Pasini and Pierini: a clinical and histopathological study

Atrophoderma of Pasini and Pierini: a clinical and histopathological study

Congenital Atrophoderma of Pasini and Pierini

Genital lichen sclerosus associated with morphoea or systemic sclerosis: clinical and HLA characteristics

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