Eosinophilic Esophageal Myositis (EoEM) Causes Jackhammer Esophagus, Rarely Posing a Problem in the Differential Diagnosis of Eosinophilic Esophagitis
Eosinophilic Esophageal Myositis (EoEM) Causes Jackhammer Esophagus, Rarely Posing a Problem in the Differential Diagnosis of Eosinophilic Esophagitis
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DOI:
10.1038/s41395-018-0171-z
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发表时间:
2018-06
期刊:
影响因子:
--
通讯作者:
Hiroki Sato-;S. Terai
中科院分区:
文献类型:
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作者:
Hiroki Sato-;S. Terai
eosinophilic infiltration in the muscle layer causes severe muscular contractions. One of the earliest reports of eosinophilic esophagitis (EoE) was in a patient with achalasia [2], and a subsequent report described a patient with esophageal spasm and eosinophilic infiltration in the muscle layer [3]. In 2015, we first reported a case of JE with eosinophilic esophageal myositis (EoEM)[4]. Among the 5 cases of EoEM (Fig. 1a), 4 were JEs and 1 was a nutcracker esophagus (NE), compatible to that reported by Tang et al. Further, EoE is a major eosinophilic disorder of the esophagus. Herein, we discuss whether patients with EoEM are easily distinguished from those with EoE.As described previously [5], our cases with EoEM-related JE/NE did not show typical endoscopic findings of EoE such as esophageal rings and white exudates. Only a compressed wall (which may be as edematous) was identified, leading to increased resistance of endoscope passage. For each patient, we performed 6 esophageal mucosal biopsies before peroral endoscopic myotomy (POEM), and no characteristic histological findings of EoE (eosinophilic infiltration≥ 15/high power field (HPF), dilated intercellular spaces, or micro-abscesses) were observed. In the latter 3 cases, during POEM, a mucosal entry site was created by cap-fitted endoscopic