Chondroid syringoma of the foot

Clinical Cases 04.01.2024
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Section: Musculoskeletal system
Case Type: Clinical Cases
Patient: 59 years, female
Authors: Quinn M. Cottone 1, Anthony L. Fortin 2, Youssef Al Hmada 3, Robert W. Morris 4
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AI Report

Clinical History

A 59-year-old woman presented with a plantar foot mass that is present for 15 years. She has a history of a tumour debulking surgery 12 years ago. The mass is painful when standing or walking.

Imaging Findings

Radiographs demonstrate well-defined erosions of the cuboid, navicular, anterior calcaneus, and intermediate and lateral cuneiforms.

Axial PD FS and sagittal T2 FS MR images demonstrate a lobulated, mildly heterogeneous, hyperintense lesion in the deep plantar soft tissue of the foot, with erosion into the surrounding bones. The mass has heterogeneous, primarily low T1 signal intensity. The mass partially encases the flexor hallucis longus and flexor digitorum longus tendons. Contrast-enhanced T1 images show diffuse enhancement of the mass.

Histopathology images at low and high magnification show nests of epithelioid cells on a background of myxoid and chondroid stroma.

Discussion

Chondroid syringoma (CS), also known as cutaneous mixed tumour, is a skin appendageal tumour of sweat gland origin, usually found in the head and neck region and much less commonly found in the extremities [1]. CS has an incidence of  <0.098% and most commonly affects middle-aged or older males [2]. CS is morphologically identical to pleomorphic adenoma of the salivary glands.

The typical presentation is a slow-growing, firm nodule in the dermis or subcutaneous fat. Prior case reports have shown a heterogeneous T2 hyperintense and T1 hypointense mass on MRI, with enhancement following contrast administration [1,2]. While it is most commonly benign, rare cases have been shown to be malignant [3]. Since malignant CS is uncommon, there are currently no concrete criteria to determine benign versus malignant CS when analyzing histopathology [4].

At pathology, there is extensive chondroid and/or myxoid stroma, with nests of epithelioid cells that have abundant eosinophilic cytoplasm and vesicular nuclei [5].

Whether benign or malignant, it has been found that surgical excision with wide margins is often curative [5], with no requirement for radiation or systemic therapy for benign disease. Once excised, the sample can be analyzed for evidence of malignancy. Although there are no well-defined criteria for malignant CS, findings such as pleomorphism, mitoses, and cytoplasmic atypia may indicate malignancy [3]. Adjuvant radiation therapy has been utilized in the treatment of rare malignant tumours [3]. In this case, there were no features of malignancy, and the patient had no evidence of tumour recurrence on one-year follow-up MRI.

As a skin appendageal tumour, chondroid syringoma is uncommonly a radiologic diagnosis. However, due to the potential for deep growth, CS can be included in the differential diagnosis for an infiltrative mass in the extremities.

Written informed patient consent for publication has been obtained.

Differential Diagnosis List

Sarcoma
Gout
Chronic granulomatous infection
Benign chondroid syringoma
Tenosynovial giant cell tumour
Lymphoma

Final Diagnosis

Benign chondroid syringoma

Figures

Lateral radiograph

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Soft tissue mass (arrowheads) with erosions of the calcaneus, cuboid, and navicular (arrows).

PA and oblique radiographs

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Erosions of the cuboid, navicular, anterior calcaneus, and intermediate and lateral cuneiforms (arrows).

Sagittal T2 fat sat

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Lobulated soft tissue mass with heterogeneous T2 signal hyperintensity.

Axial PD fat sat

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Lobulated soft tissue mass with heterogeneous PD signal hyperintensity, eroding into the anterior calcaneus (arrows). Reactive marrow oedema in the cuboid (arrowheads).

Coronal T1 without and with contrast

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The infiltrative mass demonstrates heterogeneous T1 signal intensity, with diffuse enhancement on the post-contrast fat sat T

Sagittal T1 fat sat with contrast

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Diffuse enhancement of the soft tissue mass.

H&E stain at 40x

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Nodular aggregates of epithelioid cells (arrows) distributed in a myxoid/chondroid matrix.

H&E stain at 200x

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Nodular aggregates of plump epithelioid or ovoid cells (arrows) with vesicular nuclei and prominent eosinophilic cytoplasm wi