Total: 10 |
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PMID (PMCID) | ||
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25024556 (4095635) |
OTHER | |
Chronic desquamative gingivitis in siblings: A report of two cases. | ||
Vijayakar HN, Shah PP, Desai AB, Ghonasgi SR, Gawankar RJ. J Indian Soc Periodontol. 2014;18(3):385-9. |
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A variety of diseases such as lichen planus, pemphigus, pemphigoid, dermatitis herpetiformis, linear IgA disease, lupus erythematosus, erythema multiformae manifest clinically as desquamative gingivitis. | ||
17674585 |
MALE | Middle Aged |
Drug-induced linear immunoglobulin A bullous dermatosis mimicking Stevens-Johnson syndrome: a case report. | ||
Cummings JE, Snyder RR, Kelly EB, Raimer SS. Cutis. 2007;79(3):203-7. |
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Idiopathic LABD and drug-induced LABD are clinically indistinguishable and can resemble bullous pemphigoid, dermatitis herpetiformis, or bullous erythema multiforme. | ||
17973893 |
FEMALE | Middle Aged |
Porphyria cutanea tarda in pre-existent lupus erythematosus--is there an association? | ||
van Tuyll van Serooskerken AM, Habets JM, Badeloe S, Poblete-Gutierrez P, Frank J. Int J Dermatol. 2007;46 Suppl 3:50-2. |
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However, in some instances such efflorescences might suggest an association with distinct cutaneous diseases, including erythema multiforme, toxic epidermal necrolysis or autoimmune blistering disorders such as bullous pemphigoid, pemphigus vulgaris, and dermatitis herpetiformis Duhring. | ||
15550142 |
MALE | |
Vancomycin-induced linear IgA bullous disease presenting as toxic epidermal necrolysis. | ||
Waldman MA, Black DR, Callen JP. Clin Exp Dermatol. 2004;29(6):633-6. |
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Linear IgA bullous dermatosis (LABD) is a rare autoimmune vesiculobullous disorder characterized by variable clinical presentations that may mimic bullous pemphigoid, dermatitis herpetiformis, cicatricial pemphigoid and erythema multiforme. | ||
8692084 |
FEMALE | Adult |
[Systemic diseases: evaluation of important laboratory parameters in 3 cases with unusual skin changes]. | ||
Jovanovic M, Lenert P, Poljacki M, Mitic I, Duran V. Med Pregl. 1996;49(3-4):133-6. |
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Our third case was a 21-year old female with a systemic lupus erythematous--Rowell syndrome, with skin lesions of erythema multiforme type with some similarities to dermatitis herpetiformis on the first examination. | ||
8569641 |
FEMALE | Child |
[Chronic bullous dermatoses of childhood in the differential diagnosis of bullous dermatitis in children]. | ||
Buffoni S, Salvai M. Minerva Pediatr. 1995;47(10):409-15. |
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Among those we discuss on clinical and anatomopathological aspects of Dermatitis herpetiformis, Erythema multiforme, Pemphigus and Pemphigoid, with regard to different anatomic sites of bullous lesions and to pathogenesis involved immunoglobulins and skin antigens. | ||
3316076 |
FEMALE | Middle Aged |
Linear IgA bullous dermatosis mimicking erythema multiforme in adult. | ||
Argenyi ZB, Bergfeld WF, Valenzuela R, McMahon JT, Tomecki KJ. Int J Dermatol. 1987;26(8):513-7. |
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Light microscopy revealed features of bullous pemphigoid, dermatitis herpetiformis, and erythema multiforme; immunoelectron microscopy demonstrated IgA deposition beneath the lamina densa about anchoring fibrils. | ||
6342155 |
FEMALE | Infant |
Chronic bullous dermatosis of childhood. | ||
Tomecki KJ. South Med J. 1983;76(5):651-3. |
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The disease may resemble bullous impetigo, bullous erythema multiforme, dermatitis herpetiformis, or pemphigus. | ||
7008639 |
MALE | Middle Aged |
Hodgkin's disease with specific bullous lesions. | ||
Hanno R, Bean SF. Am J Dermatopathol. 1980;2(4):363-6. |
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A variety of bullous eruptions have been reported in patients with Hodgkin's disease, among them erythema multiforme, herpesvirus infections, bullous impetigo, prurigo-like papules with vesicles, drug eruptions, bullous pemphigoid, dermatitis herpetiformis, and acquired epidermolysis bullosa. | ||
133599 |
MIXED_SAMPLE | Middle Aged |
[Chronic mucosynechial pemphigoid: so-called ocular pemphigus]. | ||
Zingirian M. Adv Ophthalmol. 1976;32:134-94. |
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At various times it has been identified with pemphigus vulgaris, dermatitis herpetiformis of Duhring-Brocq, erythema multiforme of Hebra, Stevens-Johnson syndrome, syphilitic dermatitis bullosa and other bullous dermatoses. |