Rice Thomas W, Goldblum John R, Yearsley Martha M, Shay Steven S, Reznik Scott I, Murthy Sudish C, Mason David P, Blackstone Eugene H
Department of Thoracic and Cardiovascular Surgery, Cleveland Clinic, Cleveland, OH, USA.
Eur J Cardiothorac Surg. 2009 Jan;35(1):22-7; discussion 27. doi: 10.1016/j.ejcts.2008.09.025. Epub 2008 Nov 8.
To (1) categorize histologic esophageal myenteric plexus abnormalities in patients undergoing surgical treatment for epiphrenic diverticulum, and (2) correlate histologic changes with associated esophageal motility disorders and hiatal hernia.
From January 1987 to May 2008, 40 patients had surgery for epiphrenic diverticulum. Esophageal manometry was abnormal in 29 (73%); 23 (58%) had hiatal hernia. Esophageal muscle specimens were evaluated for ganglion cell number, myenteric inflammations and myenteric fibrosis.
Myenteric plexus abnormalities were present in 31 (78%). Ganglion cells were reduced in 8 (20%) and absent in 13 (33%). Myenteric inflammation was present in 21 (53%) and myenteric fibrosis in 9 (23%). Abnormalities were seen in 10 (83%) with motility disorders only, 5 (83%) with hiatal hernia only, 13 (76%) with both, and 3 (60%) with neither. Abnormalities in diffuse esophageal spasm (n=3) were similar to those of achalasia (n=14). Ineffective esophageal motility (n=6) was strongly associated with hiatal hernia, and abnormalities were similar to those of hiatal hernia without motility disorders (n=6). All patients with nutcracker esophagus (n=3) had hiatal hernia and histologic abnormalities, and two patients with hypertensive lower esophageal sphincter (n=3, hiatal hernia in 2) had myenteric inflammation.
Myenteric plexus abnormalities predominate in epiphrenic diverticulum. Disease-specific patterns exist, but are incomplete. These associations and patterns point to causes of distal obstruction, with some commonality. In the absence of associated disorders, myenteric plexus abnormalities may be the sole finding. Isolated epiphrenic diverticulum is uncommon and may reflect an inability to detect abnormalities by current investigative techniques.
(1)对接受膈上憩室手术治疗患者的食管肌间神经丛组织学异常进行分类,(2)将组织学变化与相关食管动力障碍及食管裂孔疝进行关联分析。
1987年1月至2008年5月,40例患者接受了膈上憩室手术。29例(73%)食管测压异常;23例(58%)有食管裂孔疝。对食管肌肉标本进行神经节细胞数量、肌间炎症和肌间纤维化评估。
31例(78%)存在肌间神经丛异常。8例(20%)神经节细胞减少,13例(33%)神经节细胞缺失。21例(53%)存在肌间炎症,9例(23%)存在肌间纤维化。仅存在动力障碍的患者中有10例(83%)出现异常,仅存在食管裂孔疝的患者中有5例(83%)出现异常,同时存在两者的患者中有13例(76%)出现异常,两者均不存在的患者中有3例(60%)出现异常。弥漫性食管痉挛患者(n = 3)的异常情况与贲门失弛缓症患者(n = 14)相似。无效食管动力患者(n = 6)与食管裂孔疝密切相关,其异常情况与无动力障碍的食管裂孔疝患者(n = 6)相似。所有胡桃夹食管患者(n = 3)均有食管裂孔疝和组织学异常,2例食管下括约肌高压患者(n = 3,2例有食管裂孔疝)存在肌间炎症。
膈上憩室中肌间神经丛异常占主导。存在疾病特异性模式,但并不完整。这些关联和模式指出了远端梗阻的原因,存在一些共性。在无相关疾病的情况下,肌间神经丛异常可能是唯一发现。孤立性膈上憩室并不常见,可能反映了当前检查技术无法检测到异常情况。