Rare Diseases Symptoms Automatic Extraction

Bullous mastocytosis in a 3-month-old infant.

[cutaneous mastocytosis]

Mastocytosis is a rare myeloid neoplasm characterized by abnormal proliferation and accumulation of mast cells in one or more organ systems including the skin, bone marrow, liver, spleen, lymph nodes and gastrointestinal tract. An infant presenting with bullous lesions is an even rarer clinical presentation of cutaneous mastocytosis. The symptoms and complications are mostly in proportion to the mast cell degranulation in tissues. Management is focused on preventing and treating this event. We report a three-month-old infant with bullous mastocytosis to enhance awareness about this rare diagnosis.

Diseases presenting "gastrointestinal tract" symptom

  • benign recurrent intrahepatic cholestasis
  • carcinoma of the gallbladder
  • cowden syndrome
  • cutaneous mastocytosis
  • dedifferentiated liposarcoma
  • epidermolysis bullosa simplex
  • erdheim-chester disease
  • esophageal adenocarcinoma
  • esophageal carcinoma
  • familial mediterranean fever
  • hirschsprung disease
  • malignant atrophic papulosis
  • megacystis-microcolon-intestinal hypoperistalsis syndrome
  • proteus syndrome
  • pyomyositis
  • triple a syndrome
  • waldenström macroglobulinemia
  • well-differentiated liposarcoma

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