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 "bone marrow" symptom

  • adrenomyeloneuropathy
  • allergic bronchopulmonary aspergillosis
  • cohen syndrome
  • cushing syndrome
  • cutaneous mastocytosis
  • erdheim-chester disease
  • erythropoietic protoporphyria
  • focal myositis
  • hodgkin lymphoma, classical
  • krabbe disease
  • legionellosis
  • liposarcoma
  • monosomy 21
  • oculocutaneous albinism
  • omenn syndrome
  • papillon-lefèvre syndrome
  • pyomyositis
  • scrub typhus
  • severe combined immunodeficiency
  • systemic capillary leak syndrome
  • waldenström macroglobulinemia
  • werner syndrome
  • wiskott-aldrich syndrome

You can validate or delete this automatically detected symptom