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01.12.2016 | Case report | Ausgabe 1/2016 Open Access

World Journal of Surgical Oncology 1/2016

Pneumatosis intestinalis after gefitinib therapy for pulmonary adenocarcinoma: a case report

World Journal of Surgical Oncology > Ausgabe 1/2016
Ai Maeda, Masao Nakata, Katsuhiko Shimizu, Takuro Yukawa, Shinsuke Saisho, Riki Okita


Pneumatosis intestinalis (PI) is relatively rare finding characterized by the presence of gas within the intestinal wall. This can be caused by bowel ischemia, mechanical trauma, inflammatory disease, autoimmune disease, intestinal neoplasm, obstructive pulmonary disease, thromboembolism, or several medications [ 13]. Recently, molecular-targeted drugs have been shown to cause gastrointestinal toxicity, including PI perforation, enteritis, and fistula formation [ 1, 46]. Anti-epidermal growth factor receptors such as cetuximab and erlotinib have been reported to be associated with PI; however, only a few cases have been reported in association with gefitinib treatment [ 1, 79]. This is a report of PI associated with gefitinib therapy.

Case presentation

An 80-year-old female patient with recurrent lung cancer was admitted to our hospital because of anorexia, abdominal distension, and constipation. She had been diagnosed with recurrent left lung cancer with multiple bone metastases. She had been treated with oral gefitinib for about 6 weeks, which appeared to stabilize the disease. Her past medical history included rheumatoid arthritis (RA), cor pulmonale, bronchial asthma, and hypothyroidism, which were all under medical control. She was receiving prednisolone (PSL, 10 mg/day) for RA treatment. An abdominal X-ray showed an abnormal intestinal gas shadow (Fig.  1), and computed tomography (CT) revealed intestinal dilation with diffuse thickening of practically the entire intestinal wall, intramural gas, and intraperitoneal free air, indicating PI (Fig.  2). We selected conservative treatment with I.V. antibiotics because the increase in inflammatory parameters in the blood samples was mild (white blood cell (WBC), 8430/μL; C-reactive protein (CRP), 7.11 mg/dL; pH, 7.337; and lactate, 0.87 mEq/L) and no signs of sepsis, free gas near the portal vein, or bowel perforation were detected. We discontinued the oral intake of all drugs including gefitinib.
We speculated that this patient’s PI was induced by PSL therapy; however, it was not possible to decrease the amount of PSL because of RA. The symptoms gradually improved, and a follow-up abdominal X-ray revealed decreased intramural air (Fig.  3). Considering the good response of lung cancer to gefitinib, the drug was restarted; however, within 2 weeks of gefitinib re-initiation, the patient redeveloped marked abdominal distention, and extensive pneumatosis led to drug cessation.
The same episode occurred three times during gefitinib therapy. We discontinued the administration of gefitinib after PI recurred the third time and the patient did not experience further episodes after discontinuing the drug.


PI is a condition of extraluminal gas predominantly localized to the submucosal and subserosal planes of the intestine, but it can also be found in the muscularis propria.
Multiple theories exist for the cause of PI onset. Three different possibilities for the source of gas within the intestinal wall have been considered, including intraluminal gas, pulmonary gas, and gas produced by bacteria. Mucosal damage, increased intraluminal pressure, or both contribute to PI. Mucosal damage may result from inflammation, a defect in the gut barrier function, and steroid- or molecular-targeted therapy. Many PI-associated conditions have been described with immunosuppressive therapy as a possible causative factor. It has been suggested that long-term administration of corticosteroids induces atrophy of the intestinal mucosa, which sometimes results in a mucosal defect and subsequent translocation of gas into the submucosal layer [ 1012]. We initially speculated that PSL treatment was the cause of PI. However, considering the fact PI recurred after the initiation of gefitinib therapy, we concluded that gefitinib therapy led to PI, although the underlying mechanism is not well understood.
Several recent reports have suggested that PI is associated with molecular targeted therapy agents such as vascular endothelial growth factor (VEGF) inhibitors, tyrosine kinase inhibitors (TKI), mammalian target of rapamycin (mTOR) inhibitors, and immune modulators [ 1]. Molecular-targeted therapies can be beneficial for treating cancers but can often induce severe bowel toxicity. This effect is particularly true with VEGF inhibitors such as bevacizumab, which has been shown to increase the risk of perforation. It has been hypothesized that the decreased blood supply caused by angiogenesis inhibition may reduce the capillary density of intestinal villi, possibly causing abdominal hypoxia and microperforation and allowing air to infiltrate the bowel wall [ 1, 5].
In general, gefitinib has a good toxicity profile among the targeted molecular therapy agents. However, some patients develop specific and severe toxicities because these molecular targets also affect normal cells. Although gefitinib is generally well tolerated, its most commonly reported toxicities concern the gastrointestinal tract (diarrhea, nausea, and vomiting) and skin (rash, acne, dry skin, and pruritus). Severe gastrointestinal toxicity caused by gefitinib is uncommon, and only 1 % of patients receiving gefitinib therapy develop grade 3 or 4 diarrhea [ 9, 13]. To the best of our knowledge, only a few studies, including the current case report, have reported the association between PI and gefitinib [ 8, 9].
Most cases of PI are asymptomatic or mild; however, in the present case, the patient’s symptoms were anorexia and abdominal distension. Patients with PI most frequently present with vomiting, abdominal distension, and abdominal discomfort [ 14]. These diagnoses are made radiographically and not by symptoms. Conservative management is preferable; however, in cases involving elevated CRP or WBC levels as well as signs of sepsis, bowel perforation, or free gas near the portal vein, immediate surgery is indicated [ 1316]. In this case, the patient’s CRP levels remained at higher than normal levels on account of RA. Because we did not observe intestinal perforation or an increase in WBC levels, we selected conservative treatment.


This is a rare case report of PI caused by gefitinib. The symptoms of PI appear to be minor; however, this condition has the potential to lead to intestinal perforation. Although this complication is extremely rare, physicians should be aware of the risk of PI in patients undergoing gefitinib therapy.


CT, computed tomography; mTOR, mammalian target of rapamycin; PI, pneumatosis intestinalis; PSL, prednisolone; RA, rheumatoid arthritis; TKI, tyrosine kinase inhibitor; VEGF, vascular endothelial growth factor

Authors’ contributions

All authors have been involved in the management of the patient and in the conception of the manuscript. MN has been involved in drafting the manuscript or revising it critically for important intellectual content. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Ethics approval and consent to participate

Written informed consent was obtained from the patient’s son for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
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