Fibroma of tendon sheath of the hand in a 3-year-old boy: a case report

被引:8
|
作者
Shibayama, Hiroki [1 ,2 ]
Matsui, Yuichiro [1 ,2 ]
Kawamura, Daisuke [1 ,2 ]
Urita, Atsushi [1 ,2 ]
Ishii, Chikako [1 ,2 ]
Kamishima, Tamotsu [3 ]
Nishida, Mutsumi [4 ]
Shimizu, Ai [5 ]
Iwasaki, Norimasa [1 ,2 ]
机构
[1] Hokkaido Univ, Fac Med, Dept Orthoped Surg, Kita Ku, Kita 15 Nishi 7, Sapporo, Hokkaido 0608638, Japan
[2] Hokkaido Univ, Grad Sch Med, Kita Ku, Kita 15 Nishi 7, Sapporo, Hokkaido 0608638, Japan
[3] Hokkaido Univ, Fac Hlth Sci, Kita Ku, Kita 12 Nishi 5, Sapporo, Hokkaido 0600812, Japan
[4] Hokkaido Univ Hosp, Diagnost Ctr Sonog, Div Lab & Transfus Med, Kita Ku, Kita 14,Nishi 5, Sapporo, Hokkaido 0608648, Japan
[5] Hokkaido Univ Hosp, Dept Surg Pathol, Kita Ku, Kita 14,Nishi 5, Sapporo, Hokkaido 0608648, Japan
关键词
Fibroma of tendon sheath; Soft tissue tumor of a young child's hand; Preoperative imaging study; Case report; GIANT-CELL TUMOR;
D O I
10.1186/s12891-020-03728-x
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
BackgroundFibroma of tendon sheath (FTS) is a rare benign soft tissue tumor that often occurs in the upper extremities. It manifests as a slow-growing mass, often without tenderness or spontaneous pain. FTS occurs most commonly in people aged 20-40years and is extremely rare in young children. Because FTS presents with atypical physical and imaging findings, it might be misdiagnosed as another soft tissue tumor such as a ganglion cyst or tenosynovial giant cell tumor (TSGCT). Although marginal resection is usually performed, a high rate of local recurrence is reported.Case presentationA boy aged 3years and 1month visited our outpatient clinic with a complaint of a mass of the left hand. An elastic hard mass approximately 20mm in diameter could be palpated on the volar side of his left little finger. This mass was initially diagnosed as a ganglion cyst at another hospital. Ultrasonography revealed a well-circumscribed hypoechoic mass with internal heterogeneity on the flexor tendon. On magnetic resonance imaging (MRI), the mass showed iso signal intensity to muscle on T1-weighted images, and homogeneously low signal intensity to muscle on T2-weighted images. The mass was peripherally enhanced after contrast administration. FTS was initially suspected as the diagnosis on the basis of these imaging features. Because of the limited range of motion of his little finger, surgery was performed when he was 4years old. Histopathological findings indicated the mass was well-circumscribed and contained scattered spindle cells embedded in a prominent collagenous matrix. The spindle cells contained elongated and cytologically bland nuclei with a fine chromatin pattern. Nuclear pleomorphism and multinucleated giant cells were not observed. On the basis of these findings, we made a diagnosis of FTS. One year after surgery, no signs of local recurrence were observed.ConclusionsWe experienced an extremely rare case of FTS in the hand of a 3-year-old child. We especially recommend ultrasonography for hand tumors of young children to diagnose or eliminate ganglion cysts. MRI helped differentially diagnose FTS from TSGCT. Although marginal resection can be performed as a treatment, great care should be taken postoperatively because FTS has a high possibility of local recurrence.
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页数:6
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