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The Turkish Journal of Gastroenterology |
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2009, Volume 20, No 4, Page(s) 282-286 |
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| Hemorrhagic Meckel's diverticulum in an older woman diagnosed by repeated angiographies |
| Jee Suk LEE1, Won MOON1, Seun Ja PARK1, Moo In PARK1, Kyu Jong KIM1, Sang Ho LEE2, Hee Kyung CHANG3, Gyu Sik JUNG4 |
| Departments of 1Internal Medicine, 2General Surgery, 3Pathology, and 4Radiology, Kosin University, College of Medicine, Busan, South Korea |
| Keywords: Meckel diverticulum, hemorrhage, angiography, laparoscopy. |
| Summary |
Meckel's diverticulum is a remnant of the vitelline duct and a congenital anomaly of the gastrointestinal tract. Hemorrhage from a Meckel's diverticulum is common in children but extremely rare in adults over 50 years of age. Very few cases have been reported to date and all prior cases were in men. Meckel's diverticulum is commonly overlooked as a possible cause of a lower gastrointestinal hemorrhage in adults. Here, we present the rare case of a 58-year-old woman with massive hemorrhage from a Meckel's diverticulum that was diagnosed by repeated emergency angiographies and treated with elective laparoscopic surgery. |
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| Introduction |
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Meckel's diverticulum is a remnant of the vitelline duct and the most common congenital anomaly of the gastrointestinal tract (1). It occurs in 2-3% of the population and rarely becomes symptomatic; it has a lifetime complication rate of 4-6% (2, 3). Among patients with symptomatic Meckel's diverticulum, the male-female ratio has been reported to be approximately 3:1 (3). The major complications include inflammation, hemorrhage, intussusception, small bowel obstruction, and neoplasm (2, 3). Hemorrhage from Meckel's diverticulum is common in children but extremely rare in adults over 50 years of age (4-6). Meckel's diverticulum is usually overlooked as a possible cause of lower gastrointestinal hemorrhage in adults (4-6). We report the case of a 58-yearold woman with a gastrointestinal hemorrhage secondary to a Meckel's diverticulum diagnosed by repeated emergency angiographies and treated with elective laparoscopic surgery. |
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| Case Presentation |
A 58-year-old woman was admitted to our department on an emergency basis because of a sudden onset of hematochezia immediately after straining with a normal bowel movement. The patient denied abdominal pain and prior episodes of bloody stools. There was no significant medical or family history. There was no history of alcohol intake, or non-steroidal antiinflammatory drug (NSAIDs) or tobacco use. The patient had a resting tachycardia, but blood pressure was normal. No abnormal findings were noted on the physical examination or laboratory tests except for slightly increased bowel sounds and a decreased hemoglobin (9.3 g/dl). Nasogastric lavage yielded clear gastric fluid. Two units of packed red blood cells were immediately transfused and an urgent colonoscopy was performed without bowel preparation. A large amount of dark blood and clots were present in the entire left colon and rectum; the right colon could not be examined due to the presence of excessive blood. The following day, the patient had another episode of massive hematochezia and the hemoglobin dropped even further to 5.6 g/dl; her blood pressure dropped to 90/60 mmHg and a tachycardia of 110/min was present. The patient was transfused with six units of packed red blood cells and three units of fresh frozen plasma. A second colonoscopy without bowel preparation was performed. A large amount of fresh blood was present along the entire colon and flowed out from the terminal ileum; however, no definite bleeding focus could be found. Under 100/70 mmHg blood pressure, an emergency angiography of the superior mesenteric artery (SMA) was performed concurrently with the blood transfusion, but showed no abnormality (Figure 1). A third episode of massive hematochezia occurred on the third hospital day. The hemoglobin was 7.8 g/dl. The blood pressure dropped to 85/55 mmHg and a tachycardia of 115/min was present. An immediate transfusion was required; however, there was no blood available specific for this patient in the blood banks within about 200 km of our hospital. Before taking the decision of the last exploratory laparotomy, as a final attempt at a diagnosis and treatment for the bleeding, a second emergency selective superior mesenteric angiography was performed. At first, the angiographic findings were negative. However, repeated infusions of intra-arterial contrast medium concurrently with rapid intravenous infusion of normal saline (until reaching a blood pressure of 130/80 mmHg) revealed a single elongated, non-branching arcade of an abnormal ileal artery arising from the distal SMA with intermittent extravasations of the contrast medium (Figures 2A, 2B). This artery was thought to be the vitellointestinal artery, a feeding artery of Meckel's diverticulum. Immediate embolization was carried out successfully with Gelfoam particles and two coils. After the procedure, the vital signs promptly stabilized to 140/90 mmHg and the pulse rate to 76/min. For protection from recurrent bleeding, a curative elective laparoscopic surgery without blood transfusion was performed three hours later. A 4.0 cm-long and 2.0 cm-wide Meckel's diverticulum was noted at about 50 cm proximal to the ileocecal junction on the antimesenteric side; it was resected with a laparoscopic stapler (Figure 3A). Multiple hemorrhagic erosions and small ulcers were noted in the resected specimen (Figure 3B). The pathology findings confirmed the diagnosis of Meckel's diverticulum and heterotopic gastric mucosa with ulcers (Figure 4A, 4B). The patient had no postoperative complications and was discharged on postoperative day 7; there have been no further episodes of gastrointestinal bleeding over the one-year follow-up.
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| Discussion |
The causes of obscure small intestinal hemorrhage in adults include angiodysplasia, a small bowel tumor, Crohn's disease, and NSAID-induced ulcers (7). However, hemorrhage from a Meckel's diverticulum is very rare in the adult age group (7). Mackey et al. (8) reviewed 402 patients with Meckel's diverticulum. Only 16.9% of the patients were symptomatic and one- quarter of them had gastrointestinal hemorrhage; the oldest was 31 years of age (8). There are only three cases of hemorrhagic Meckel's diverticulum that have been reported in patients more than 50 years of age, at 53, 68 and 91 years (9-11). They were all men. Therefore, this case is the first report of hemorrhagic Meckel's diverticulum in a woman over 50 years of age. In our case, the diverticular wall had ectopic gastric mucosa with ulcerations. More than 80% of hemorrhagic diverticula contain ectopic gastric mucosa (4). This acidic environment may lead to ulcer formation within the diverticulum and this is the likely reason for gastrointestinal hemorrha- 284 LEE et al. ge (4). The hemorrhage is usually painless, as in our case12. The hemorrhage can be massive and dramatic, manifesting as bright red blood in the stool, or it can be slow and occult, manifesting as anemia (12). We performed repeated emergency angiographies under the unstable vital signs but did not consider Meckel's diverticulum as a possible cause of the massive hemorrhage since it would be extremely rare given our patient's age. Tc99mpertechnetate scanning is known as one of the most useful diagnostic methods for the diagnosis of Meckel's diverticulum with heterotopic gastric mucosa (13). The diagnostic accuracy is more than 90% in children and only 50% to 65% in adults (13). However, this procedure cannot be performed in an emergency status, as was the case with our patient. Angiography of the mesenteric artery is helpful during active gastrointestinal hemorrhage (14). The confirmation of the diagnosis of hemorrhage is made when contrast medium extravasation occurs into the bowel lumen. However, it is difficult to find the bleeding site when the rate of bleeding is less than 0.5 ml/min (14). However, in cases of Meckel's diverticulum, where the bleeding might be intermittent, the demonstration of an abnormal embryonic artery might be the most noticeable finding (15). Such a finding indicates the high probability of Meckel’s diverticulum, even without extravasation, of a bleeding focus (15). The embryonic artery is characteristically a single, enlarged, elongated, unbranched anastomotic arcade originating from an ileal branch, or from the ileocolic artery of the distal SMA (16). In this case, even the abnormal vasculature was not visualized in the initial angiography under the low blood pressure. This suggests the probability of not only a lower rate of bleeding than 0.5 ml/min or intermittent bleeding (14), but also spasm of the abnormal feeding artery, which had a physiologic response to bleeding and low systemic intravascular volume with low blood pressure (15). We used the rapid intravenous infusion of normal saline to fill the intravascular volume and raise the blood pressure against the circulatory collapse. The diagnostic rate of angiography, for gastrointestinal hemorrhage, has been reported to be between 40% and 78% (17). Repeated angiography might be useful to localize a bleeding focus in patients with gastrointestinal bleeding of obscure origin who have a negative initial angiography (18). We successfully detected an abnormal feeding artery of Meckel's diverticulum by repeated angiography with rapid intravascular volume-filling in an extreme situation when no blood for transfusion was available. In conclusion, we report the first case of a massive hemorrhagic Meckel's diverticulum in an older woman over 50 years of age, diagnosed by repeated emergency angiographies and treated with an elective laparoscopic surgery. |
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| References |
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1. Moore TC. Omphalomesenteric duct malformations. Semin Pediatr Surg 1996; 5: 116-23. 2. Fink AM, Alexopoulou E, Carty H. Bleeding Meckel's diverticulum in infancy: unusual scintigraphic and ultrasound appearances. Pediatr Radiol 1995; 25: 155-6. 3. Park JJ, Wolff BG, Tollefson MK, el al. Meckel diverticulum: the Mayo Clinic experience with 1476 patients (1950- 2002). Ann Surg 2005; 241: 529-33. 4. Vane DW, West KW, Grosfeld JL. Vitelline duct anomalies: experience with 217 childhood cases. Arch Surg 1987; 122: 542-7. 5. Mujica VR, Barkin JS. Occult gastrointestinal bleeding. General overview and approach. Gastrointest Endosc Clin N Am 1996; 6: 833-45. 6. Mackey WC, Dineen P. A fifty year experience with Meckel's diverticulum. Surg Gynecol Obstet 1983; 156: 56-64. 7. Zuckerman GR, Prakash C, Askin MP, Lewis BS. AGA technical review on the evaluation and management of occult and obscure gastrointestinal bleeding. Gastroenterology 2000; 118: 201-21. 8. Mackey WC, Dineen P. A fifty year experience with Meckel's diverticulum. Surg Gynecol Obstet 1983; 156: 56-64. 9. Haimov M, Rybak BJ, Greenberg EI, Dreiling DA. Lower gastrointestinal bleeding due to ulcerations in a Meckel's diverticulum and adjacent ileum with enteroliths formation. Am J Gastroenterol 1972; 58: 497-501. 10. Lichtstein DM, Herskowitz B. Massive gastrointestinal bleeding from Meckel's diverticulum in a 91-year-old man. South Med J 1998; 91: 753-4. 11. Stone PA, Hofeldt MJ, Lohan JA, et al. A rare case of massive gastrointestinal hemorrhage caused by Meckel's diverticulum in a 53-year-old man. W V Med J 2005; 101: 64-6. 12. Turgeon DK, Barnett JL. Meckel' s diverticulum. Am J Gastroenterol 1990; 85: 771-81. 13. Kusumoto H, Yoshida M, Takahashi I, el al. Complications and diagnosis of Meckel's diverticulum in 776 patients. Am J Surg 1992; 164: 382-3. 14. Kusumoto H, Kumashiro R, Masuda Y, Inutsuka S. Preoperative diagnosis of Meckel's diverticulum in a 62-yearold man: utility of an angiographic technique. Radiat Med 1993; 11: 17-20. 15. Marx FW Jr, Gray RK, Duncan AM, Bakhtiar L. Angiodysplasia as a source of intestinal bleeding. Am J Surg 1977; 134: 125-30. 16. Mitchell AW, Spencer J, Allison DJ, Jackson JE. Meckel's diverticulum: angiographic findings in 16 patients. AJR Am J Roentgenol 1998; 170: 1329-33. 17. Zuccaro G Jr. Management of the adult patient with acute lower gastrointestinal bleeding. American College of Gastroenterology. Practice Parameters Committee. Am J Gastroenterol 1998; 93: 1202-8. 18. Lau WY, Ngan H, Chu KW, Yuen WK. Repeat selective visceral angiography in patients with gastrointestinal bleeding of obscure origin. Br J Surg 1989; 76: 226-9. |
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References
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