A 56-year-old woman presented to our hospital with right lower quadrant pain. She experienced pain once every few months beginning a few years previously. Her abdomen was soft, with no peritoneal irritation signs or palpable masses. An abdominal contrast-enhanced computed tomography (CT) revealed a thickened appendix (1.5 cm in diameter) and some focal calcifications in the appendiceal wall. Abnormal findings were not seen in the terminal ileum. There was no evidence of tumor and no acute inflammatory signs (Fig. 1). Colonoscopy showed no mucosal lesions in the appendiceal orifice and cecum. Owing to the lack of findings requiring emergency treatment, we followed her without therapy for 2 months. After 2 months, we performed an abdominal contrast-enhanced CT again because her abdominal pain did not alleviate. The findings in the appendix were the same as those obtained earlier. We then assumed that the patient had chronic appendicitis and performed a laparoscopic surgery to diagnose and treat the condition.
Intraoperative findings included purple-colored, granular lesions that were raspberry-like in appearance and were spread diffusely along the surface of the appendix (Fig. 2a). These lesions spread to the terminal ileum (Fig. 2b, c). Therefore, laparoscopic ileocecal resection was performed to completely resect the lesion. The resected ileocecum contained approximately 6 cm of the ileum (Fig. 2d). She was discharged with an uneventful postoperative course. After surgery, her abdominal pain alleviated.
Macroscopic inspection of the resected specimen revealed purple-colored, raspberry-like lesions, which were spread diffusely on the serosal surface of the appendix. No lesions were found on the mucosal surface (Fig. 3a). Histological examination indicated that there were large and small sinus-like spaces, largely in the subserosal layer. The same finding was also observed in the submucosal and proper muscular layer (Fig. 3b). Some of these spaces were filled with blood (Fig. 3c). Cells that lined the vascular spaces were strongly immunoreactive for CD34, which is one of the main markers of endothelial cells (Fig. 3d). These sinus-like spaces were thought to be malformed vessels. Although there was chronic inflammation in the mucosal layer of the appendix, the structure of the mucosal layer was not injured. Finally, we diagnosed the patient with diffuse cavernous vascular malformation of the appendix.
Discussion
As shown in this case, unexplained chronic right lower quadrant pain and appendiceal wall thickening with focal calcification, as evidenced by CT, may possibly be a case of CHA, which is otherwise difficult to diagnose preoperatively. Owing to limited available reports, clinical manifestations and findings of various diagnostic images of CHA are not well-known. Previously, CHA was reported to cause no symptoms. For this reason, it was only incidentally discovered during a surgery to treat other lesions [3, 5]. Another report indicated that intraperitoneal bleeding was caused by rupture of the CHA, which was also not diagnosed preoperatively [6]. Another case was reported along with acute appendicitis, which was diagnosed preoperatively [7]. Previous reports involving diagnostic imaging demonstrated that CT, magnetic resonance imaging (MRI), and colonoscopy were unable to detect the lesion [5]. Meanwhile, in other reports, no diagnostic imaging modalities were employed and CHA was not diagnosed preoperatively [3, 6]. Gastrointestinal cavernous hemangiomas can cause pain and gastrointestinal bleeding [8, 9]. Furthermore, CT imaging can detect focal calcification in gastrointestinal hemangioma as a degenerative change [10]. Gastrointestinal endoscopy, including esophagogastroduodenoscopy, colonoscopy, and capsule endoscopy, can also be useful diagnostic tools for gastrointestinal cavernous hemangioma [8]. While the chronic right lower quadrant pain and the appendiceal wall thickening with focal calcifications that were observed by CT in this study have not been described for CHA previously, they corroborate the pathology of CHA. It is possible that obstruction of the appendiceal lumen and congestion of the intestinal fluid in the appendix can cause abdominal pain. Since a colonoscopy can reveal only the appendiceal orifice, this examination might not fully contribute to a diagnosis of CHA. However, a colonoscopy may also be necessary to rule out other possible diseases such as cancer or inflammatory diseases.
This case also demonstrates that laparoscopic surgery can be a useful tool for both diagnosis and treatment. Diagnostic laparoscopy for suspected appendicitis has been shown to be useful for its diagnosis and treatment because it is usually a simple and safe procedure that is helpful in obtaining other diagnoses [11]. CHA has specific findings, such as a purple-colored nodular or granular lesion that is raspberry-like in appearance, which can be seen only during surgery [3, 5]. In the present case, the same finding was observed and laparoscopic resection was performed. A conservative surgical resection, such as laparoscopic surgery, was thought to be a sufficient treatment in order to relieve symptoms or prevent complications caused by CHA. To the best of our knowledge, this is the first report wherein CHA was observed and resected using a laparoscopic approach.
Similarly, cavernous vascular malformation of the mesoappendix has been reported [9, 12, 13]. Like CHA, cavernous vascular malformation of the mesoappendix is a rare disease and can form a tumor that results in abdominal pain. CT and MRI can provide informative findings for diagnosis. The relationship between appendiceal cavernous hemangioma and mesoappendicial cavernous hemangioma are not well known. To better understand the pathophysiology, further clinical data are required.
