Calcified Leiomyoma of the Distal Forearm in a Child: A Case Report and Review of Literature
Background. Deep somatic leiomyomas arising in skeletal muscle are extremely rare in children, especially in the extremities. Around half of them show calcifications. We present a rare case of a calcified leiomyoma of the distal forearm in a child. Case Summary. A seven-year-old boy presented with r...
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2020-01-01
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Series: | Case Reports in Orthopedics |
Online Access: | http://dx.doi.org/10.1155/2020/8821265 |
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doaj-7801ed4329da4a41a7f6c1dc7d57594f2020-11-25T01:25:41ZengHindawi LimitedCase Reports in Orthopedics2090-67492090-67572020-01-01202010.1155/2020/88212658821265Calcified Leiomyoma of the Distal Forearm in a Child: A Case Report and Review of LiteratureNadeeke Nidhan Perera0Sunil Ranjith Wijayasinghe1Karuna Dissanayake2Jerard Fernando3Ethige Tharushi De Silva4National Hospital of Sri Lanka, Colombo, Sri LankaLady Ridgeway Hospital for Children, Colombo, Sri LankaNational Hospital of Sri Lanka, Colombo, Sri LankaLady Ridgeway Hospital for Children, Colombo, Sri LankaColombo North Teaching Hospital, Ragama, Sri LankaBackground. Deep somatic leiomyomas arising in skeletal muscle are extremely rare in children, especially in the extremities. Around half of them show calcifications. We present a rare case of a calcified leiomyoma of the distal forearm in a child. Case Summary. A seven-year-old boy presented with right distal forearm and wrist pain with restricted supination for 4 years. X-ray showed ring and arc calcifications in the distal forearm at the interosseous area. MRI also confirmed a well-defined soft tissue lesion with areas of calcifications. A diagnosis of a cartilage-forming lesion or a peripheral nerve sheath tumour was suggested. The lesion was completely excised. Histology showed a lesion composed of intersecting fascicles of spindle cells with stromal calcification having immunohistochemical features of a leiomyoma. Conclusion. Although soft tissue calcifications can be seen in a plethora of conditions seen in daily orthopaedic practise, a high index of suspicion should be maintained for rare conditions like deep somatic leiomyoma.http://dx.doi.org/10.1155/2020/8821265 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nadeeke Nidhan Perera Sunil Ranjith Wijayasinghe Karuna Dissanayake Jerard Fernando Ethige Tharushi De Silva |
spellingShingle |
Nadeeke Nidhan Perera Sunil Ranjith Wijayasinghe Karuna Dissanayake Jerard Fernando Ethige Tharushi De Silva Calcified Leiomyoma of the Distal Forearm in a Child: A Case Report and Review of Literature Case Reports in Orthopedics |
author_facet |
Nadeeke Nidhan Perera Sunil Ranjith Wijayasinghe Karuna Dissanayake Jerard Fernando Ethige Tharushi De Silva |
author_sort |
Nadeeke Nidhan Perera |
title |
Calcified Leiomyoma of the Distal Forearm in a Child: A Case Report and Review of Literature |
title_short |
Calcified Leiomyoma of the Distal Forearm in a Child: A Case Report and Review of Literature |
title_full |
Calcified Leiomyoma of the Distal Forearm in a Child: A Case Report and Review of Literature |
title_fullStr |
Calcified Leiomyoma of the Distal Forearm in a Child: A Case Report and Review of Literature |
title_full_unstemmed |
Calcified Leiomyoma of the Distal Forearm in a Child: A Case Report and Review of Literature |
title_sort |
calcified leiomyoma of the distal forearm in a child: a case report and review of literature |
publisher |
Hindawi Limited |
series |
Case Reports in Orthopedics |
issn |
2090-6749 2090-6757 |
publishDate |
2020-01-01 |
description |
Background. Deep somatic leiomyomas arising in skeletal muscle are extremely rare in children, especially in the extremities. Around half of them show calcifications. We present a rare case of a calcified leiomyoma of the distal forearm in a child. Case Summary. A seven-year-old boy presented with right distal forearm and wrist pain with restricted supination for 4 years. X-ray showed ring and arc calcifications in the distal forearm at the interosseous area. MRI also confirmed a well-defined soft tissue lesion with areas of calcifications. A diagnosis of a cartilage-forming lesion or a peripheral nerve sheath tumour was suggested. The lesion was completely excised. Histology showed a lesion composed of intersecting fascicles of spindle cells with stromal calcification having immunohistochemical features of a leiomyoma. Conclusion. Although soft tissue calcifications can be seen in a plethora of conditions seen in daily orthopaedic practise, a high index of suspicion should be maintained for rare conditions like deep somatic leiomyoma. |
url |
http://dx.doi.org/10.1155/2020/8821265 |
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