-transparent.png){kind=logo}
Mastocytosis is a disorder of unknown etiology characterized by an abnormal proliferation of tissue mast cells, and/or by degranulation of abnormally behaving mast cells that show no proliferation, but release myriad active metabolites. This results in a wide spectrum of signs and symptoms that fluctuate considerably. The presently available diagnostic tests vary in their specificity and sensitivity. We have evaluated the role of radiologic studies in 78 confirmed cases of systemic mastocytosis and/or mastocytosis-like syndrome, including barium meal and small bowel follow-through (UGI-SBFT).
Related Publications
A C Johnson, and
S Johnson, and
P D Lester, and
S Halter, and
E James
December 2008,
World journal of gastroenterology,
A C Johnson, and
S Johnson, and
P D Lester, and
S Halter, and
E James
July 2010,
Inflammatory bowel diseases,
A C Johnson, and
S Johnson, and
P D Lester, and
S Halter, and
E James
January 1979,
Mayo Clinic proceedings,
A C Johnson, and
S Johnson, and
P D Lester, and
S Halter, and
E James
February 1997,
Radiology,
A C Johnson, and
S Johnson, and
P D Lester, and
S Halter, and
E James
October 1985,
Orthopedics,
A C Johnson, and
S Johnson, and
P D Lester, and
S Halter, and
E James
July 1983,
The American journal of surgical pathology,
A C Johnson, and
S Johnson, and
P D Lester, and
S Halter, and
E James
July 2021,
Cancers,
A C Johnson, and
S Johnson, and
P D Lester, and
S Halter, and
E James
June 1999,
American family physician,
A C Johnson, and
S Johnson, and
P D Lester, and
S Halter, and
E James
July 1990,
AJR. American journal of roentgenology,
A C Johnson, and
S Johnson, and
P D Lester, and
S Halter, and
E James
August 2022,
World journal of gastroenterology,
