An extremely rare case of neuromuscular and vascular hamartoma of the appendix

被引:2
|
作者
Sasaki, Takahiro [1 ]
Furuhata, Tomohisa [1 ]
Nishimura, Masashige [1 ]
Ono, Tatsunori [1 ]
Noda, Akiyoshi [1 ]
Koizumi, Hirotaka [2 ]
Miyajima, Nobuyoshi [1 ]
Otsubo, Takehito [3 ]
机构
[1] St Marianna Univ, Digest Dis Ctr, Toyoko Hosp, Sch Med,Nakahara Ku, 3-435 Kosugicho, Kawasaki, Kanagawa, Japan
[2] St Marianna Univ, Dept Pathol, Toyoko Hosp, Sch Med,Nakahara Ku, 3-435 Kosugicho, Kawasaki, Kanagawa, Japan
[3] St Marianna Univ, Sch Med, Dept Gastroenterol & Gen Surg, Miyamae Ku, 2-16-1 Sugao, Kasawaki, Japan
关键词
Appendix; Neuromuscular and vascular hamartoma; SMALL-BOWEL; SMALL-INTESTINE; PATHOLOGICAL OVERLAP; DIAPHRAGM DISEASE;
D O I
10.1186/s40792-020-00970-2
中图分类号
R61 [外科手术学];
学科分类号
摘要
BackgroundNeuromuscular and vascular hamartoma is a rare lesion of the small intestine, with only 26 cases reported since its initial description in 1982. No occurrence of hamartoma in the appendix has been reported until now.Case presentationA 60-year-old man had been suffering from longstanding right lower quadrant pain. Abdominal computed tomography showed a slight swelling of the appendix as the possible cause of his pain. Laparoscopic appendectomy with partial resection of the cecum was performed for diagnostic and therapeutic purposes. An 18 x 10-mm lesion located on the tip of the appendix was found in the resected specimen. Pathological examination showed that the lesion was covered with normal mucosa and consisted of adipose tissue, smooth muscle fibers, small vessels, and neural fibers. These findings were consistent with neuromuscular and vascular hamartoma of the appendix.ConclusionThis is the first report of neuromuscular and vascular hamartoma arising from the appendix.
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页数:5
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