A patient with spontaneous rupture of the esophagus and concomitant gastric cancer whose life was saved: case of report and review of the literature in Japan
© Matsuhashi et al; licensee BioMed Central Ltd. 2011
Received: 18 July 2011
Accepted: 6 December 2011
Published: 6 December 2011
A 71-year-old man suddenly developed abdominal pain and vomiting on drinking soda after a meal, and visited a physician. Cervical subcutaneous and mediastinal emphysemas were observed on CT, and the patient was transferred to the emergency medical center of our hospital on the same day. Esophagography was performed at our department. A ruptured region was identified on the left side of the lower thoracic esophagus, and surgery was emergently performed employing sequential left thoracoabdominal incision. The chest wall was adhered due to inflammation, and large amounts of residual food and sloughing were present in the thoracic cavity and mediastinum. Moreover, necrotic changes were noted in the superior through inferior mediastinum. An about 2-cm rupture site was confirmed on the left side of the lower thoracic esophagus and closed by suture and filling with pediculate omentum. The presence of a tumorous lesion located mainly in the body of the stomach and lymph node enlargement were also diagnosed before surgery, for which gastric and intestinal fistulae were inserted to prepare for the second-stage surgery. The patient was admitted to an ICU after surgery. ARDS and MRSA-induced pneumonia and enteritis concomitantly developed but remitted. Curative surgery for gastric cancer was performed at 40 POD. Spontaneous rupture of the esophagus is relatively rare and that complicated by gastric caner is very rare, with only six cases being reported in Japan. Herein, we report the case.
Keywordsspontaneous rupture of the esophagus gastric cancer prediagnoisis
Spontaneous rupture of the esophagus is rare, and the life-saving rate is still low. We encountered a very rare case in which rupture occurred due to concomitant gastric cancer. Only 6 cases including this patient have been reported in Japan, and this is the first case report in English. The disease could be preoperatively diagnosed, and the patient could be saved despite the condition being very serious. Herein, we report the case.
The patient was a 71-year-old male with a chief complaint of abdominal pain. There was no particular past medical history. The patient suddenly developed abdominal pain and vomiting on drinking soda after a meal, and visited a physician. Cervical subcutaneous and mediastinal emphysemas were observed on CT, and the patient was transferred to the emergency medical center of our hospital on the same day. On admission, the height was 168 cm; body weight, 55 kg; BP, 154/76 mmHg; HR, 93/min; respiratory rate, 35/min; and SpO2, 98% (O2 5 L mask). The patient could not hold a supine position due to respiratory distress and pain. On blood testing and chemistry on admission, WBC was 14.5 × 103/ul and CRP was 0.34 mg/dl, showing high levels of inflammatory parameters. BUN was 46 mg/dl and Cr was 4.03 mg/dl, revealing features of prerenal renal failure. PT-INR was 1.35; AT-III, 63%; and FDP, 64 μg/ml. CEA was 11.7 ng/ml, showing a high level.
The ruptured site was identified on the left side of the lower thoracic esophagus on esophagography and diagnosed as spontaneous rupture of the esophagus. Surgery was emergently performed in consideration of concomitant gastric cancer.
In spontaneous rupture of the esophagus, a sharp rise in intraesophageal pressure due to vomiting causes full-thickness (mucosa and muscle layer) rupture. Since the disease was initially reported by Boerhaave  of Holland in 1724, it is also called Boerhaave syndrome1). In Japan, Yoshida et al. reported it in 1935, and several cases have been reported thereafter. The mortality rate was higher than 40% and gradually decreased, but the outcomes of treatment are still unfavorable compared to other diseases, and the prognosis is particularly poor in patients brought to hospital in a state of shock.
There is a high incidence in men, accounting for 92% of all cases. The onset age peaks in the 40s, and incidences at 30-59 years of age account for 73% of all cases. The rupture site was located in the lower esophagus in 84% and left wall in 67%, and the most frequent inducer was vomiting (64%) followed by other mechanical factors, such as overeating, cough, and trauma, accounting for 19% .Regarding the diagnosis, awareness of this disease may lead to early diagnosis. Actually, only about 30% of cases were diagnosed as rupture of the esophagus. When it is suspected, esophagography is performed using an aqueous contrast medium, Gastrografin, and the disease is definitely diagnosed when leakage in the mediastinum or thoracic cavity is observed. As CT has recently spread, noninvasive CT may be useful, especially for patients in a state of shock. MDCT may also be useful for assistive diagnosis of the lesions.
For treatment, surgery and conservative treatment including thoracic cavity drainage are available, but surgical treatment may be the most appropriate . Fukushima et al. reported that the mortality rates after surgical and conservative treatments were 7.7 and 50.0%, respectively, showing unfavorable outcomes in the conservative treatment group .
In our patient, not only rupture of the esophagus but also hypertrophy of the antral stomach wall and lymph node swelling were observed on preoperative MDCT, for which sequential left thoracoabdominal incision (oblique incision) was selected. Gastric (to reduce pressure) and intestinal (for tube nutrition) fistulas were inserted, in addition to drainage, providing useful for postoperative enteric nutrition.
Of cases assumed to be induced by vomiting, duodenal ulcer was the most frequent cause, and gastric ulcer, postgastrectomy disorder, and congenital obstruction are included in the causes. In this patient, in addition to the underlying vulnerability of the esophageal wall and promotion of nausea and vomiting, the pylorus was obstructed by gastric cancer as a local factor of nausea and vomiting. Under these conditions, ingestion of the meal and soda may have rapidly elevated the inner pressure and caused rupture.
Reported cases of Spontaneous rupture of the esophagus with gastric cancer in Japan
Spontaneous rupture of the esophagus associated with concomitant gastric cancer are rare.To our knowledge this is the first reported case.
Written informed consent was obtained from the patient for publication of this case report and accompanying images.A copy of the written consent is available for review by the Editor-in-Chief of this journal.
- Boerhaave's Atroicis,descrips,morbid histroria: The first translation of the classic case report of rupture of the esophagus,with annotation. Bull Med libr. 1955, 43: 217-240.Google Scholar
- Yoshida T: Guhatuseisyokudouharetsu no 1rei(in Japanese). Kaigunikaishi. 1935, 24: 97-98.Google Scholar
- Kijima M, Aoki T, Nagao F: Experiences in the diagnosis and treatment of spontaneous rapture of the esophagus. A case of rapture concomitant with a gastric cancer -with a review of preexisting proemetic factors reported in japan-1987-Tokyo Jikeikai Medical J. 1987, 102: 1483-1987.Google Scholar
- Abot OA, Mansour KA, Longan WD: Atraumatic so-called "spontaneous"rupture of esophagus,a review of 47 personal cases with commnts on new method of surgical therapy. J Thorac Cardiovasc Surg. 1970, 59: 67-83.Google Scholar
- Fukushima J, Nabeya K, Hanaoka T: Hozontekikaryou de tiryoushita tokuhatuseisyokudouharetsu no 1rei(in Japanese). Kyurin I kaishi. 1988, 19: 455-460.Google Scholar
- De Schipper JP, Pull ter Ginne AF, Oostvogel HJ: Spontaneus rupture of the oesopagus:Boerhaave's syndrome in 2008.Literature review and treatment algorithm. Dig Surg. 2009, 26 (1): 1-6. 10.1159/000191283.View ArticlePubMedGoogle Scholar
- Landen S, EI Nakadi I: Minimally inavasive approach to Boerhaave's syndrome:a pilot study of three cases. Surg Endosc. 2002, 16 (9): 1354-1357. 10.1007/s00464-001-9185-4.View ArticlePubMedGoogle Scholar
- Lawrence DR, Ohri SK, Moxon RE: primary esophageal repair for Boerhaave's syndrome. Ann Thorac Surg. 1999, 67 (3): 818-820. 10.1016/S0003-4975(99)00043-0.View ArticlePubMedGoogle Scholar
- Fiscon V, porrale G, Friqo F: Spontaneous rupture of middle thoracic esophagus:thoracoscopisc treatment. Surg Endosc. 2010, 24 (11): 2900-2902. 10.1007/s00464-010-1056-4.View ArticlePubMedGoogle Scholar
- Teh E, Edwards J, Duffy J: Boerhaave's syndorome:a review of management and outcome:Interract Cardiovasc Tharac Surg. 2007, 6 (5): 640-643.Google Scholar
- Yoshida K, Ide H, Yamana : Igan ni heipatushita tokhatuseisyokudouharetsu no 1tikenrei(in Japanese). Geka. 1981, 8: 875-879.Google Scholar
- Emoto k, Nomiura T, Takahashi T: A case of spontaneous rapture of the esophagus associated with an early gastric cancer. J of Transportation Med. 1996, 50: 175-178.Google Scholar
- Itano S, Terada N, Hashimoto O: Igan saitoinshi toshite hassyoushita tokuhatuseisyokudouharetsu no 1rei(in Japanese). Ringeka. 1992, 53: 1619-1623.Google Scholar
- Kaneshiro E, Hanatani Y, Miyoshi H: A case of spotaneuos rupture of the esophagus combined with gastric cancer. Teikyo Med J. 1999, 22: 363-368.Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.