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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Main Authors: Nadeeke Nidhan Perera, Sunil Ranjith Wijayasinghe, Karuna Dissanayake, Jerard Fernando, Ethige Tharushi De Silva
Format: Article
Language:English
Published: Hindawi Limited 2020-01-01
Series:Case Reports in Orthopedics
Online Access:http://dx.doi.org/10.1155/2020/8821265
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spelling 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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