scholarly journals Ulcerated Keloid Secondary to a Coexisting Complicated Epidermal Inclusion Cyst: A Sonographic Diagnosis

2020 ◽  
Vol 36 (4) ◽  
pp. 365-368
Author(s):  
Jaime Pérez-Wilson ◽  
Carolina Whittle ◽  
Viviana García ◽  
Frances Norris ◽  
Alex Castro ◽  
...  

Keloid is a benign fibroblastic tumor that is most often secondary to tissue injury. The clinical presentation is a hard red or purple tumor, mostly itchy or painful. The clinical objectives are to report an ulcerated keloid secondary to a central or inner complicated epidermal inclusion cyst histologically proven and to describe the sonographic findings that permitted the diagnosis. A 29-year-old man with multiple large keloids on the chest wall presented with a two-day pain history, increased volume, and ulceration on one side. Physical examination showed a keloid with edema, peripheral erythema, and a 1-cm central ulcer with purulent discharge. On the sonogram, multiple solid dermal hypodermal pseudotumors were visualized. The lesions were well-defined hypoechogenic heterogeneous solid masses that were hypovascular with color Doppler, concordant with keloids. Within the ulcerated enlarged mass, a complicated epidermal inclusion cyst was discovered with inflammatory changes. The significance of this case lies in the very low frequency of ulceration of a keloid and the high diagnostic value of sonography to demonstrate the presence of a coexisting epidermal inclusion cyst. In the differential diagnosis of an ulcerated keloid, sonography can assist in achieving a better presurgical approach.

1974 ◽  
Vol 109 (2) ◽  
pp. 251-252 ◽  
Author(s):  
K. E. Greer

1998 ◽  
Vol 171 (6) ◽  
pp. 1709-1710 ◽  
Author(s):  
A R Fisher ◽  
P H Mason ◽  
K S Wagenhals

2018 ◽  
Vol 10 (1) ◽  
pp. 61-68 ◽  
Author(s):  
Ethan Frank ◽  
David Macias ◽  
Brian Hondorp ◽  
Justin Kerstetter ◽  
Jared C. Inman

Epidermal inclusion cysts are common lesions that rarely develop into squamous cell carcinoma (SCC). Neoplastic change in these cysts can be associated with prominent symptoms such as pain, rapid growth, or ulceration. This study describes the case of a 64-year-old woman with a 4-year history of a largely asymptomatic neck mass, which after routine excision was found to be an epidermal inclusion cyst harboring well-differentiated SCC. The diagnosis was made incidentally after routine cyst bisection and hematoxylin and eosin staining. Given the potential for variable presentation and low cost of hematoxylin and eosin analysis, we recommend a low threshold for a comprehensive pathological search for malignancy in excised cysts when appropriate.


2012 ◽  
Vol 42 (2) ◽  
pp. 219-224 ◽  
Author(s):  
Afshin Mohammadi ◽  
Mohammad Ghasemi-rad ◽  
Miramir Aghdashi ◽  
Nikol Mladkova ◽  
Paria Baradaransafa

Rare Tumors ◽  
2014 ◽  
Vol 6 (3) ◽  
pp. 114-115 ◽  
Author(s):  
Brijesh Thakur ◽  
Sanjeev Kishore ◽  
Aparna Bhardwaj ◽  
Sandip Kudesia

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