The Journal of Foot & Ankle Surgery xxx (2015) 1–6

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Case Reports and Series

Chondroid Syringoma of the Foot: A Rare Diagnosis Khaled Madi, DPM 1, Alicia Attanasio, DPM 1, Fejzo Cecunjanin, DPM 1, Roberto A. Garcia, MD 2, Alexander Vidershayn, MD 3, Jeffrey V. Lucido, DPM, FACFAS 4 1

Resident Physician, Department of Podiatric Medicine and Surgery, Lutheran Medical Center, Brooklyn, NY Associate Professor, Division of Bone and Soft Tissue Pathology, Department of Pathology, Mount Sinai School of Medicine, New York, NY 3 Attending Radiologist, Department of Radiology, Lutheran Medical Center, Brooklyn, NY 4 Chief, Department of Podiatric Medicine and Surgery, and Director, Podiatric Medical Education, Lutheran Medical Center, Brooklyn, NY 2

a r t i c l e i n f o

a b s t r a c t

Level of Clinical Evidence: 4

Chondroid syringoma is a rare tumor with the potential for malignant transformation and distant metastasis. The site of predilection for benign chondroid syringoma is the head and neck region, and it is less likely to involve the foot. In contrast, malignant chondroid syringoma is more commonly encountered in the extremities and is characterized by rapid growth, local invasion, and distant metastasis. We report an unusual case of benign chondroid syringoma in a 47-year-old female who presented with a 20-year history of a mass in her left foot to bring such cases to the attention of foot and ankle specialists. We highlight the histologic diagnosis and surgical procedures with a 6-month postoperative follow-up period. It is unlikely that a treating physician would anticipate this histologic tumor type, considering the rarity of the condition, the long history of this patient’s lesion, and the benign presentation in the extremities. Ó 2015 by the American College of Foot and Ankle Surgeons. All rights reserved.

Keywords: benign lower extremity malignant neoplasm pleomorphic adenoma skin tumor

Pleomorphic adenoma, or chondroid syringoma (CS), is a rare benign skin appendageal tumor (1,2). Originally described by Bilmuth in 1859, Hirsch and Helwig (3) were the first to use the term “chondroid syringoma” to this tumor type in the early 1960s and described the presence of sweat gland elements in cartilaginous stroma (4–6). CS is rare among primary skin tumors, with a reported incidence of 2 cm, a rapidly growing mass, or the development of pain in a previously painless mass (3). In our patient, the indications for excision were the patient’s report of recent relative rapid enlargement of the lesion in the 2 years before her July 2012 visit and the atypical presentation of the lesion on MRI. Because of the potential for malignant transformation, total excision of CS is the preferred treatment modality for the benign form of the tumor. For malignant CS, the recommended treatment is wide resection of the tumor with regional lymph node dissection (3,17,21,27). Because it is a lobulated type of tumor, it has been recommended to include normal tissue margins to ensure that the entire tumor has been removed (5,28). Although local radiotherapy is often unsuccessful, skeletal metastasis has been shown to respond to radiotherapy. Combination

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Chondroid Syringoma of the Foot: A Rare Diagnosis.

Chondroid syringoma is a rare tumor with the potential for malignant transformation and distant metastasis. The site of predilection for benign chondr...
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