Literature DB >> 6387670

Bullous mastocytosis: diffuse cutaneous mastocytosis with extensive blisters mimicking scalded skin syndrome or erythema multiforme.

L E Golitz, W L Weston, A T Lane.   

Abstract

Bullous mastocytosis (diffuse cutaneous mastocytosis) is a rare form of mast cell disease that begins during the first month of life and causes extensive blisters that mimic scalded skin syndrome or bullous erythema multiforme. Discrete pigmented macules, papules, and nodules are absent and the characteristic leathery induration of skin may not develop until 6 months of age. Skin biopsy shows a subepidermal blister with mast cells at the base. The most serious complications are gastrointestinal hemorrhage and shock. The symptoms of bullous mastocytosis may be modified by a number of new therapeutic agents.

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Year:  1984        PMID: 6387670     DOI: 10.1111/j.1525-1470.1984.tb01131.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  3 in total

Review 1.  Development of mast cells and importance of their tryptase and chymase serine proteases in inflammation and wound healing.

Authors:  Jeffrey Douaiher; Julien Succar; Luca Lancerotto; Michael F Gurish; Dennis P Orgill; Matthew J Hamilton; Steven A Krilis; Richard L Stevens
Journal:  Adv Immunol       Date:  2014       Impact factor: 3.543

2.  Occurrence of platelet-activating factor (PAF) and an endogenous inhibitor of platelet aggregation in diffuse cutaneous mastocytosis.

Authors:  J L Macpherson; A Kemp; M Rogers; A I Mallet; R F Toia; B Spur; J W Earl; C N Chesterman; S A Krilis
Journal:  Clin Exp Immunol       Date:  1989-09       Impact factor: 4.330

3.  Oral and topical sodium cromoglicate in the treatment of diffuse cutaneous mastocytosis in an infant.

Authors:  Alan Martin Edwards; Stepánka Capková
Journal:  BMJ Case Rep       Date:  2011-06-29
  3 in total

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