Lipoid proteinosis

Konstantinov, Konstantin; Kabakchiev, Petko; Karehev, Todor; Kobayasi, T; Ullman, S

doi:10.1016/0190-9622(92)70183-g

Cited by 32 publications

(17 citation statements)

References 22 publications

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“…Uptake and retention of [ 35 S0 4 ] proteo- glycans were reported to be higher in cultured fibroblasts from the lesion than in normal skin fibroblasts (4). In the present study, as well as in previous studies by ourselves and others (15)(16)(17)(18)(19)(20)(21), inclusion bodies were neither mentioned nor adequately demonstrated in fibroblasts of the lesion, either in vivo or in vitro. Cultured fibroblasts from Case #1 produced many electrondense inclusion bodies; however, control normal fibroblasts in culture also produced the same inclusion bodies.…”

Section: Discussioncontrasting

confidence: 73%

Late Onset Hyalinosis Cutis et Mucosae

Hashimoto

Wang

et al. 2000

The Journal of Dermatology

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Two cases of non-familial, late onset (50 and 62-years-old) hyalinosis cutis et mucosae were studied and compared with classical early onset cases. Late onset cases showed essentially the same histological and ultrastructural features described for early onset cases. The late onset variety should be distinguished from other diseases; they resemble systemic amyloidosis and sometimes the adult form of colloid milium.

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Section: Discussioncontrasting

confidence: 73%

Late Onset Hyalinosis Cutis et Mucosae

Hashimoto

Wang

et al. 2000

The Journal of Dermatology

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“…The characteristic histological findings include extensive deposits of amorphous eosinophilic material in the papillary dermis, along the capillaries 1 . The hyaline material stains strongly with PAS, indicating the presence of glycoproteins 6 .…”

Section: Discussionmentioning

confidence: 99%

“…Lipoid proteinosis, also called hyalinosis cutis et mucosa and Urbach–Wiethe disease, is an uncommon, recessively inherited disorder characterized by non‐inflammatory, persistent papules on the skin and mucous membranes 1,2,4 …”

Section: Discussionmentioning

confidence: 99%

Lipoid proteinosis: A case with ophthalmological and psychiatric findings

Bahadır¹,

Çobanoğlu²,

Kapicioğlu

et al. 2006

The Journal of Dermatology

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Lipoid proteinosis (LP) is an uncommon, recessively inherited disorder. The disease usually has its onset in the newborn period and is manifested by hoarseness. The skin and mucous membrane involvement arises between the first and second year of age. A 14-year-old male presented with the complaint of blistering on various sites of his skin, from the age of 12 months, resulting in scarring. Ophthalmological and psychiatric findings also appeared during the clinical course. The histological findings of skin biopsy included extensive deposits of amorphous eosinophilic material in the papillary dermis. No known therapy exists for LP.

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“…Deposition of hyaline material on vocal cords can lead to hoarseness or aphonia in early life. Because of the potential for causing unsightly scars, the disease should be treated as soon as possible to enable a normal psychosocial development 1 …”

mentioning

confidence: 99%

Treatment of lipoid proteinosis with acitretin: a case report

Toosi

Ehsani

2009

Acad Dermatol Venereol

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References1 Trassard M, Le Doussal V, Hacene K et al. Prognostic factors in localized primary synovial sarcoma: a multicenter study of 128 adult patients. J Clin Oncol 2001; 19: 525-534. 2 Andrassy RJ, Okcu MF, Despa S, Raney RB. Synovial sarcoma in children: surgical lessons from a single institution and review of the literature. J Am Coll Surg 2001; 192: 305-313. 3 White BE, Kaplan A, Lopez-Terrada DH, Ro JY, Benjamin RS, Ayala AG.Monophasic synovial sarcoma arising in the vulva: a case report and review of the literature.

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Lipoid proteinosis

Cited by 32 publications

References 22 publications

Late Onset Hyalinosis Cutis et Mucosae

Late Onset Hyalinosis Cutis et Mucosae

Lipoid proteinosis: A case with ophthalmological and psychiatric findings

Treatment of lipoid proteinosis with acitretin: a case report

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