Mastocytosis refers to the increased amunt of mast cells in the system. Released mast cell mediators may induce vasodilation, hypotension, flushing, pruritus, syncope, diarrhea, fatigue, headache, cachexia, local anticoagulation, and/or tissue remodeling and fibrosis.
Systemic mastocytosis may occur at any age among adults. This disease can cause flushing, syncope, vascular collapse or anaphylaxis triggered by exercise, alcohol, aspirin and NSAIDs, morphine, narcotics and opiates, insect stings, infections or exposure to iodinated contrast and medical/surgical procedures (such as biopsies or endoscopy).
The reported frequency of GI effects varies greatly depending upon the source, ranging from 18 to 85 percent with a mean of 50 percent. Symptoms and abnormalities include abdominal pain, diarrhea, nausea, vomiting, peptic ulcer disease, and gastrointestinal bleeding. Precipitation of symptoms is common with the administration of drugs (such as narcotics, aspirin and NSAIDS, procaine, and penicillin), exposure to cold or hot temperature, barium enemas, trauma, stress, exercise, alcohol, and medical procedures (including bone marrow biopsy, laparotomy, or endoscopy).
Diagnosis would involve various tests of the bone marrow for increased amounts of mast cells. Elevations in urine histamine levels are useful for the diagnosis of systemic mastocytosis. A urinary histamine concentration above 30 ng/mL is considered abnormal, with two measurements required for diagnostic accuracy.
You may want to discuss this diagnosis with a hematologist for further evaluation.
Followup with your personal physician is essential.
This answer is not intended as and does not substitute for medical advice - the information presented is for patient education only. Please see your personal physician for further evaluation of your individual case.
Thanks,
Kevin, M.D.