A 75-year-old man with a history of colonic polyps, hypertension, childhood tonsillectomy, and a remote smoking history presented with a complaint of “excessive mucus in the throat” for the past several years. The patient had a sensation of a “sore throat” for years along with more frequent bowel movements and increased flatus. There were no other gastrointestinal complaints. The patient subsequently had maculopapular rashes which on biopsy showed increased numbers of dermal mast cells highlighted by c-kit (CD 117) immunoperoxidase staining consistent with that of dermal mastocytosis (Figure ). The haematoxylin and eosin stain (HE) is also included (Figure ).
Figure 1 The patient subsequently had maculopapular rashes which on biopsy showed increased numbers of dermal mast cells highlighted by c-kit (CD 117) immunoperoxidase staining consistent with that of dermal mastocytosis. The haematoxylin and eosin stain (HE) (more ...)
When seen by the gastroenterologist, the patient had no lymphadenopathy in the head and neck region but did have tissues in the distal soft palate and pharynx appearing uniformly swollen and hyperemic. The respiratory, cardiovascular, and neurological exams were grossly normal. On abdominal exam there was no organomegaly, masses, tenderness, or inguinal lymphadenopathy. A ventral hernia was noted.
On colonoscopy a mucus type material adherent to the mucosa was present in the right colon along with a slightly raised appearance of the mucosa through areas of the transverse and right colon (Figure ). The biopsy in these colonic regions showed an increased number of mast cells with recruited eosinophils in the lamina propria (Figure HE). The mast cells are highlighted by positive c-kit staining (Figure ).
On colonoscopy a mucus type material adherent to the mucosa was present in the right colon along with a slightly raised appearance of the mucosa through areas of the transverse and right colon.
The biopsy in these colonic regions showed an increased number of mast cells with recruited eosinophils in the lamina propria (HE).
The mast cells are highlighted by positive c-kit staining.
Common GI complaints in SM include abdominal pain, diarrhea, nausea, and vomiting[2
]. It appears that the frequency of various GI symptoms is less variable than their prevalence[2
]. These symptoms are thought to be secondary to mast cell mediators on the GI tract. The most common symptom is abdominal pain (mean 51%) followed by diarrhea (mean 43%) and nausea or vomiting (mean 28%)[2
]. Abdominal pain can be classified into two different types corresponding to different pathology. Epigastric dyspeptic pain is associated with ulcer disease and acid hypersecretion whereas no dyspeptic pain is characterized by lower abdominal cramps[8
]. Diarrhea is thought to occur due to gastric acid hypersecretion, malabsorption caused by mucosal injury and edema, and altered bowel motility[8
]. Moreover, diarrhea in SM can also be caused or contributed to by tissue infiltration by mast cells[3,9
]. It is however worth noting that the mast cells themselves do not secrete gastrointestinal peptides that directly alter motility[3
A common symptom in SM is facial flushing[10
]. The flushing in SM can be distinguished from the flushing seen in the rare but more prevalent carcinoid tumors in that carcinoid flushing is generally more widespread, patchy, violaceous, and evanescent, lasting only a few minutes, often occurs postprandially, and in the majority of cases not associated with hemodynamic changes[10
]. Furthermore, the response to long acting somatostatin analogue octreotide, the specific pattern of mediator excretion, and aggravation of the flushing by epinephrine in the carcinoid case can assist in the differentiation[10,11
]. In SM, the flushing tends to be more bright red, pruritic, and burning, and may be accompanied simultaneously by other symptoms of systemic mast cell degranulation including GI symptoms[10,12
Other symptoms may also occur as a result of GI bleeding and peptic ulcer disease[2,3
]. It is estimated that GI bleeding occurs in 11% of SM[2
]. Contrary to previously reports it is estimated that peptic ulcer disease is an under diagnosed phenomena[2
]. Indeed in a more recent prospective study within which nine patients had upper GI endoscopy, four of the nine patients had peptic ulcer disease[3
]. Interestingly, hypersecretion of gastric acid is not consistently related to the level of serum histamine levels measured[3
]. It may however be possible that a relationship between tissue concentration of histamine and GI manifestations may exist[3
]. It is unclear what triggers the vasoactive mediators from mast cells but certain medications such as NSAIDS, opiate analgesics, procaine, and penicillin may be potential triggers[13
Rarely, esophageal complaints in SM are made and include symptoms due to esophagitis and in some reports variceal bleeding secondary to portal hypertension that may develop in SM[14
Signs of GI SM include steatorrhea, malabsorption, hepatomegaly, splenomegaly[2
] and sometimes ascites secondary to portal hypertension. Steatorrhea can be measured by 72-h fecal fat excretion test, D-xylose tolerance test, and Shilling test. In SM steatorrhea is associated in 5%-67% of patients[7,15,16
]. Hepatomegaly was found in 41%-72% of patients[12,17
]. Mast cells are known to infiltrate the liver diffusely with or without portal fibrosis and rarely cirrhosis in 4% of patients[12
]. Portal hypertension is also reported in association with SM[18,19
] and is ascribed to pre- and post-sinusoidal block secondary to mast cell infiltration and or fibrosis[18
]. Splenomegaly attributable to SM is thought to be due to mast cell infiltration that may accompany hepatomegaly[20,21
]. Marked splenomegaly was found to be more common in aggressive SM[22
]. Since SM is a rare entity a low clinical suspicion is required and usually the diagnosis is made on biopsy[10
Case reports highlight some of the more unusual pathology. One such is SM and giant gastroduodenal ulcers associated with telangiectasia macularis eruptiva perstans which is thought to represent a cutaneous form of mastocytosis[8
]. Rarely aggressive SM can be complicated by protein-losing enteropathy[23
]. Other reports include initial misdiagnosis as SM can mimic inflammatory bowel disease[9,24
] and Zollinger-Ellison syndrome[24
Small intestinal pathology may reveal dilated loops of bowel and thickened, edematous or scalloped folds[6,25
]. In the colon, urticarial lesions, diverticulitis, polypoid lesions, and diffuse intestinal telangiectasia may be seen (Figure )[25,26
Diagnosis of SM is based on identification of neoplastic mast cells by morphologic, immunophenotypic, and/or genetic criteria in various organs. Specifics of the World Health Organization criteria for the diagnosis of SM based on a paper by Valent et al[27
] will not be discussed. Currently there is no consensus GI biopsy criteria.
Needless to say, patients with obvious dermatological findings are diagnosed by clinicians more quickly as having SM. Unfortunately, patients lacking skin manifestations of SM have a delayed diagnosis even though they often have more aggressive disease, impaired liver function, ascites, malabsorption, and splenomegaly[28
Interestingly our endoscopic images (Figure ) from the colonic involvement look markedly different from previously published images by Scolapio et al[25
]. In the pictures provided in this paper, the appearance of SM in the colon would be described as small mucosal nodules with focal areas of edema, urticarial, granular, and multiple purple-pigmented lesions. To date these are the first endoscopic images that contain all of these features although these findings have been reported in isolation or in pairs[25,29,30
An earlier review by Jensen in 2000 has reported the following endoscopic findings which are displayed in a table[2
]. (Table adapted from Jensen[2
Endoscopic features reported in patients with systemic mastocytosis with gastrointestinal symptoms