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MOJ
eISSN: 2374-6939

Orthopedics & Rheumatology

Case Report Volume 16 Issue 1

Isolated hemangioma of the foot

Makgabo Tladi

Louis Pasture, Jakaranda and Cure Midkin hospitals, South Africa

Correspondence: Makgabo Tladi, Louis Pasture, Jakaranda And Cure Midkin Hospitals, suite 840 louis pasture private hospital, South Africa

Received: December 25, 2023 | Published: January 8, 2024

Citation: Tladi M. Isolated hemangioma of the foot. MOJ Orthop Rheumatol. 2024;16(1):6-7. DOI: 10.15406/mojor.2024.16.00654

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Abstract

Hemangiomas are soft tissues tumors that rarely affect the feet and majority are asymptomatic. If activities of daily living is affected, treatment is indicated. The diagnosis is usually made through histopathology. We are presenting a case report of a female patient who presented with a painful and sensitive plantar mass that was treated with an excision.

Introduction

Hemangiomas are vascular, benign tumors that are usually caused by vasoformative tissue proliferation.1 They are commonly found in the neck and head. Any vascular body tissue can be affected. Some studies have reported more prevalence in females while others have shown no gender difference.2,3 They constitute about 7% to 10% of all soft tissue benign tumors.4,5 Foot and ankle involvement is reported to be rare.3,6 Compartment syndrome of the foot has been reported in a child.7 Malignant transformation is reported to be rare.8

Case report

A 42 year old female patient presented with atraumatic right foot painful plantar mass for 12 months period. The mass made her to have difficulties with shoe wear. On examination, the mass (Figure 1) was tender and sensitive to touch. The x-rays of the foot were normal. The sonar showed a well circumscribed mass. She consented for excision of the mass. Intraoperative the lesion had reddish colour with blood vessels within (Figure 2). Histology showed a vascular proliferation in the dermis that was lined by flattened endothelium. Haemosiderin pigment was identified in the surrounding stroma. The features were consistent with a diagnosis of haemangioma.

Figure 1 Medial plantar mass.

Figure 2 Hemangioma (blue arrow) with blood vessels within (orange arrows).

Discussion

Hemangiomas are frequently encountered in childhood and early adulthood. In the absence of histopathological evaluation, clinical diagnosis is often difficult to make. Majority are asymptomatic and in those that are symptomatic, about 98% present with a mass and 60% will have pain that can be made worse by activities.3,5 The condition can mimic various conditions. A case of chronic ankle pain presenting as a peroneal tenosynovitis has been described.6

Radiological investigations are often nonspecific. The x rays can either be normal or those with small lesions that extend into adjacent bones can appear as a rounded or liner areas of hyperlucency. Fewer cases can present with phlebolithis.9 On MRI T1 images, the lesion can appear as low to intermediate signal intensity containing variable amounts of high signal intensity fat. With T2 images, the lesion can show high signal intensity and a striated or septate configuration because of multiple vascular channels.5

Histological appearance of a haemangioma consists of a well circumscribed mass having proliferation of capillaries located at the matrix. The thin vessels are arranged in lobules. Various classification can be used.2

Most of these tumours do not require interventions. However, others may need interventions because of their size, pain control or near structures functional involvement. Conservative management include steroid, or sclerotherapy. Surgical management usually involves cauterization with sliver nitrate, curettage or excision.2,3 Preoperative embolization can be done if the feeding vessels are larger. Recurrence rate is reported to be about 18% to 60% if the mass is partially excised or feeding vessels are not ligated.5,10

Conclusion

Hemangiomas of the foot and ankle are rare. The condition can mick other conditions. Painful lesions may medical interventions. Surgically, the lesion needs to be completely resected to prevent recurrence.

Acknowledgments

None.

Conflicts of interest

None.

Consent

The consent to publish the case report was obtained from the patient.

References

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©2024 Tladi. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.