scholarly journals Chondroid syringoma (mixed tumour of the skin): a report of eight cases and review of the literature

2019 ◽  
Vol 3 (1) ◽  
pp. 31
Author(s):  
Hande MOLLAMEMIŞOĞLU ◽  
Faruk Erdem KOMBAK ◽  
Fatma Nihal DURMUŞ KOCAASLAN ◽  
Leyla CINEL
2006 ◽  
Vol 12 (5) ◽  
Author(s):  
Raja Sivamani ◽  
Akhil Wadhera ◽  
Errol Craig

1997 ◽  
Vol 111 (9) ◽  
pp. 862-864 ◽  
Author(s):  
Deepa Bhargava ◽  
Shivayogi Bhusnurmath ◽  
A. S. Daar

AbstractChondroid syringoma or mixed tumour of the skin is a rare benign tumour which can present on the face. We present here the case of a patient who underwent an excisional biopsy of a small painless nodule in the soft triangle of the nose for cosmetic reasons. The clinical presentation, histology and treatment, with review of the relevant literature, is discussed.


1989 ◽  
Vol 79 (11) ◽  
pp. 563-565 ◽  
Author(s):  
TG Toback ◽  
CJ Toback

The third documented case of chondroid syringoma occurring in a toe, involving the largest tumor of the three, along with a review of the literature, has been presented. The possibility of a mixed tumor should be kept in mind when considering the differential diagnosis of a solid nodule in the skin, particularly if it is of long duration. These tumors usually will present as simple, asymptomatic, subcutaneous nodules that are shelled out easily during surgical excision. However, there is a tendency toward local recurrence that usually is attributed to incomplete surgical removal, which easily may occur because of the lobulation of the tumor. Complete excision of the primary tumor always is recommended, as diagnosis can be made only by histopathologic examination. Six reported cases revealed that the recurrence of the lesion following primary excision resulted in malignant degeneration. In nine reported cases where metastasis had occurred, the initial site of metastasis in five patients was the regional lymph nodes, and, in four patients, there was metastasis in the lung. The period of time between the removal of the primary lesion and the malignant local recurrence or metastasis has been reported to be from 1 to 4 years. Recognition of chondroid syringoma is clinically difficult because of its rarity. Its diagnosis requires histologic examination.


2004 ◽  
Vol 26 (5) ◽  
pp. 403-406 ◽  
Author(s):  
Hayato Takahashi ◽  
Akira Ishiko ◽  
Masakazu Kobayashi ◽  
Akiko Tanikawa ◽  
Hiroshi Takasu ◽  
...  

2007 ◽  
Vol 65 (9) ◽  
pp. 1836-1839 ◽  
Author(s):  
Zev Schulhof ◽  
George E. Anastassov ◽  
Harry Lumerman ◽  
David Mashadian

2021 ◽  
Vol 14 (7) ◽  
pp. e232943
Author(s):  
Pujon Purkayastha ◽  
Richard Thomson ◽  
Nicholas Wilson Jones ◽  
Selwyn Ng

Coined in 1961 by Hirsch and Helwig, the term chondroid syringoma refers to a rare mixed tumour of subcutaneous tissue. Histologically, these tumours are almost identical to pleomorphic adenomas, arising from salivary glands. With the obvious difference being the presence of sweat gland tissue (syringoma) within a matrix of cartilage (chondroid). These mixed tumours remain scarce throughout the world, with an incidence of less than 0.098%. The vast majority of cases are reported in middle-aged and older adults, where they typically present as painless swellings in the head and neck, which gradually grow in size.


Author(s):  
Nechal Kaur ◽  
Neelam Gupta ◽  
Vikas Dubey ◽  
Neetu Bala

Chondroid syringoma is also known as mixed tumour of the skin. It is a rare, biphasic cutaneous neoplasm similar to pleomorphic adenoma of salivary glands. Because of its rarity, many cases are misdiagnosed in the initial stages as cysts or other cutaneous adnexal neoplasms and are often identified only after being sent for histopathological examination.Although it usually presents in middle and older aged patients, we are presenting three younger patients with Chondroid syringoma, located over the back, nose and cheek, respectively.


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