Yagan Pillay1. 1. Department of Surgery, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Abstract
Gastric gastrointestinal stromal tumours (GISTs) with cholelithiasis in the English literature are quite rare with a few published case reports. Their concurrent surgical management has also been debated as the clinical symptoms are often ascribed to one of the pathologies. All case reports to date have reported on cholesterol cholelithiasis. We would like to present a first case report of pigment cholelithiasis and a gastric GIST and their concurrent laparoscopically management. This was facilitated due to the patient's request to deal with both pathologies as well as the nebular signs concerning the symptoms that she presented with. We were able to undertake the dual surgeries without compromising her oncological outcomes. Published by Oxford University Press and JSCR Publishing Ltd.
Gastric gastrointestinal stromal tumours (GISTs) with cholelithiasis in the English literature are quite rare with a few published case reports. Their concurrent surgical management has also been debated as the clinical symptoms are often ascribed to one of the pathologies. All case reports to date have reported on cholesterol cholelithiasis. We would like to present a first case report of pigment cholelithiasis and a gastric GIST and their concurrent laparoscopically management. This was facilitated due to the patient's request to deal with both pathologies as well as the nebular signs concerning the symptoms that she presented with. We were able to undertake the dual surgeries without compromising her oncological outcomes. Published by Oxford University Press and JSCR Publishing Ltd.
Gastrointestinal stromal tumours (GISTs) are the commonest mesenchymal tumours of the gastrointestinal tract. With a recorded incidence of 0.1–3% of all gastrointestinal malignancies they remain quite rare [1]. They arise from the interstitial cells of Cajal and the majority are located in the stomach [1]. Seventy percent of gastric GISTs arise in the gastric body as in this case report [1]. Pigmented gallstones comprise between 2 and 30% of all gallstones and their aetiology involves excessive bilirubin destruction [2]. We present the following case in accordance with the CARE reporting checklist.
CASE REPORT
A 64-year-old female patient was referred for surgical consultation of her chronic abdominal pain. The pain originated in her epigastrium and radiated to the back. There was no food pain association and the nature of the pain was described as spasmodic.The pain was intermittent in nature and had been present for 1 year punctuated by the occasional emergency room visit for intravenous analgesic control. She had symptoms of dyspepsia and early post prandial satiety but no acid reflux or dysphagia.Radiology (a) CT scan coronal view showing the gallbladder filled with radiolucent stones (orange arrow) and the GIST in the stomach (green arrow). (b) CT scan axial view showing the gastric GIST in the submucosal tissue (green arrow). (c) CT scan sagittal view showing the gastric GIST on the posterior wall of the stomach (orange arrow). (d) MRI axial view showing the tumour with a pneumatocele (green arrow). (e) MRI coronal view showing the tumour on the posterior wall of the stomach (orange arrow) with the visible pneumatocele. (f) T2 weighted MRI axial view showing the GIST dimensions.Endoscopy (a) gastroscope showing the GIST on the posterior gastric wall and its relationship to the gastro-oesophageal junction. (b) second gastroscope with injection of methylene blue (yellow arrow) to mark the tumour borders. (c) mucosal ulceration due to tumour enlargement (blue arrow) on the second gastroscope 6 weeks later.An abdominal examination revealed no palpable lesions or abdominal wall hernia. She had no clinical signs of an acute abdomen. Her medical history was significant for asthma, dermatomycosis and endometriosis. Radiological imaging, with an abdominal ultrasound confirmed cholelithiasis but no cholecystitis or choledocholithiasis. The ultrasound also showed an incidental gastric lesion in the posterior wall of the stomach. A subsequent computerized tomography (CT) scan showed an isolated lesion in the posterior wall of the stomach and no obvious gastric lymphadenopathy (Fig. 1a–c). Radiolucent gallstones were also visualized on the CT scan (Fig. 1a). Differential diagnosis of the gastric lesion included a leiomyoma or a GIST. Upon discussion with an interventional radiologist, the gastric lesion was deemed radiologically inaccessible to percutaneous biopsy. A magnetic resonance imaging (MRI) scan was performed to confirm the diagnosis. MRI showed a well-circumscribed soft tissue lesion in the posterior wall of the stomach in keeping with a gastric GIST (Fig. 1d–f).
Figure 1
Radiology (a) CT scan coronal view showing the gallbladder filled with radiolucent stones (orange arrow) and the GIST in the stomach (green arrow). (b) CT scan axial view showing the gastric GIST in the submucosal tissue (green arrow). (c) CT scan sagittal view showing the gastric GIST on the posterior wall of the stomach (orange arrow). (d) MRI axial view showing the tumour with a pneumatocele (green arrow). (e) MRI coronal view showing the tumour on the posterior wall of the stomach (orange arrow) with the visible pneumatocele. (f) T2 weighted MRI axial view showing the GIST dimensions.
Surgery: laparoscopic cholecystectomy. (a) clipping of the common bile duct. (b) retrograde dissection of the fundus of the gallbladder. (c) iatrogenic gallbladder injury and spillage of pigment stones (green arrow). (d) completion of the retrograde dissection with visualization of the cystic duct stump (green arrow).Surgery: gastric wedge resection. (a) laparoscopic entry into the lesser sac through the gastro-colonic ligament (blue arrow). (b) methylene blue markings visible on the serosal layer of the stomach (blue arrows) to delineate the tumour margins. (c) complete mobilization of the gastro-colic and gastro-splenic ligament and visualization of the gastric GIST (green arrow) on the posterior wall of the stomach. (d) macroscopically clear tumour margins post GIST resection. (e) posterior gastric wall sutured closure (yellow arrow).Gross pathology. (a) mucosal view with ulceration of the gastric mucosa (orange arrow). (b) serosal view showing the gastric serosal layer.An elective gastroscope showed a soft tissue mass on the posterior wall of the body of the stomach (Fig. 2a). This appeared to be an underlying submucosal tumour with no mucosal involvement. Biopsies taken showed a normal mucosa with no malignant or premalignant mucosal pathology. A complete pathological diagnosis could not be ascertained and after an extensive discussion with the patient and her family, conservative management was contemplated rather than a surgical resection. Her symptom profile did not fit clearly with either biliary colic or a gastric GIST. Three months later the patient returned to consider surgery as the pain was not subsiding. She had a second gastroscope to mark the tumour margins with methylene blue as part of her workup for a laparoscopic gastric wedge resection (Fig. 2b). The mucosa over the lesion now showed an ulceration which we ascribed to excessive tumour growth (Fig. 2c). She also requested a concomitant laparoscopic cholecystectomy as we could not clearly elucidate the aetiology behind her abdominal pain. An informed consent was signed along with permission to record the surgical procedure. The laparoscopic cholecystectomy, initially performed, was uneventful. This was a combined antero-retrograde cholecystectomy (Fig. 3a–d). The greater curvature of her stomach was mobilized laparoscopically until the lesion was clearly visualized on the posterior wall with the aid of the methylene blue dye injected at endoscopy (Fig. 4a–c). The decision was then made to convert to open surgery and the lesion excised with a 1 cm margin (Fig. 4d). The gastrotomy wound was closed in two layers with a 2–0 polydioxanone absorbable running suture (Fig. 4e). Her physiological recovery was unremarkable, and she was discharged home on post-operative Day 5. Pathology confirmed the presence of a gastric GIST with clear surgical margins. Gallbladder pathology showed a chronic cholecystitis and pigment stones (Fig. 5).
Figure 2
Endoscopy (a) gastroscope showing the GIST on the posterior gastric wall and its relationship to the gastro-oesophageal junction. (b) second gastroscope with injection of methylene blue (yellow arrow) to mark the tumour borders. (c) mucosal ulceration due to tumour enlargement (blue arrow) on the second gastroscope 6 weeks later.
Figure 3
Surgery: laparoscopic cholecystectomy. (a) clipping of the common bile duct. (b) retrograde dissection of the fundus of the gallbladder. (c) iatrogenic gallbladder injury and spillage of pigment stones (green arrow). (d) completion of the retrograde dissection with visualization of the cystic duct stump (green arrow).
Figure 4
Surgery: gastric wedge resection. (a) laparoscopic entry into the lesser sac through the gastro-colonic ligament (blue arrow). (b) methylene blue markings visible on the serosal layer of the stomach (blue arrows) to delineate the tumour margins. (c) complete mobilization of the gastro-colic and gastro-splenic ligament and visualization of the gastric GIST (green arrow) on the posterior wall of the stomach. (d) macroscopically clear tumour margins post GIST resection. (e) posterior gastric wall sutured closure (yellow arrow).
Figure 5
Gross pathology. (a) mucosal view with ulceration of the gastric mucosa (orange arrow). (b) serosal view showing the gastric serosal layer.
We present a rare case of pigment cholelithiasis and a gastric GIST. These dual pathologies were laparoscopically managed, concurrently, with excellent oncological outcomes.
FOOTNOTE
Reporting Checklist: The authors have completed the CARE reporting checklist.
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