scholarly journals A rare case of an enlarged celiac lymph node diagnosed as an epidermal inclusion cyst

2020 ◽  
Vol 35 (2) ◽  
pp. 480-481
Author(s):  
Sung Bum Kim ◽  
Kook Hyun Kim ◽  
Tae Nyeun Kim ◽  
Chan Woo Cho ◽  
Joon Hyuk Choi
Author(s):  
NISHANT LAL ◽  
SARAN NALLASAMY ◽  
SHAFY ALI KHAN

Epidermal cysts are congenital lesions that originate from embryonal tissue remnants. It requires histopathology for its diagnosis. In this case, we report a young male with no comorbidities presenting with perianal swelling. He was evaluated and taken up for surgery. Post operative period was uneventful and he was discharged on 2nd post operative day. He is doing well at 4 months of follow up.


2021 ◽  
Vol 26 (1) ◽  
pp. 27-32
Author(s):  
Jae Young Chun ◽  
Si-Gyun Roh ◽  
Jong-Lim Kim ◽  
Jin Yong Shin ◽  
Suk Choo Chang ◽  
...  

Interdigitating dendritic cell sarcoma (IDCS) is an extremely rare neoplasm that usually arises in lymph nodes, but also can exist in extranodal sites. This report is about a case study of IDCS in the upper arm skin with axillary lymph node metastasis. A 66-year old woman had a slowly growing mass with tenderness sensation on her right upper arm that was being injected triamcinolone acetonide at local clinic. The presumptive diagnosis was a ruptured epidermal inclusion cyst, and empiric antibiotic therapy was done; however, she had poor respondence to antibiotic therapy. Therefore, magnetic resonance imaging, incisional biopsy, positron emission tomography-computed tomography, and bone scan were performed and a malignant tumor was diagnosed. She received surgical resection and lymph node dissection of the right axilla. No adjuvant chemotherapy was done. Although extremely rare, this case suggests that extranodal IDCS should be considered in differential diagnosis of untreated atypical skin mass and early biopsy should be performed.


Heliyon ◽  
2020 ◽  
Vol 6 (6) ◽  
pp. e04225
Author(s):  
Y. Houcine ◽  
A. Sassi ◽  
M. Mlika ◽  
H. Yassine ◽  
F. Mezni

2020 ◽  
Vol 6 (4) ◽  
pp. 20200038
Author(s):  
Peter Lauffer ◽  
Joost van Schuppen ◽  
Christiaan F. Mooij

An epidermal/(epi)dermoid cyst of the thyroid is a rare cause of an intrathyroidal mass. At radiological evaluation, it may initially be misinterpreted as a thyroid adenoma or carcinoma. We present a case report of a 15-year-old boy, who was evaluated because of a neck mass which caused globus pharyngeus and pain at swallowing. Ultrasound examination revealed a hypoechoic nodule-like structure in the left thyroid lobe. Aspiration of the nodule yielded white fluid. Cytological evaluation confirmed the diagnosis of an epidermal inclusion cyst of the thyroid.


2021 ◽  
Vol 49 (3) ◽  
pp. 030006052199767
Author(s):  
Yongxia Zhang ◽  
Lei Song ◽  
Han Zhang ◽  
Fengjie Liu ◽  
Guo Hao ◽  
...  

Epidermal inclusion cysts (EICs) of the breast develop in the deep breast parenchyma, and they are very rare. Only about 10 cases have been reported in the English-language literature to date. In this report, we present a rare case of a giant EIC with infection arising within the deep breast parenchyma. Unlike a typical EIC of the breast, the EIC in the present case was a cystic and solid lesion containing a large amount of liquid within the cyst and popcorn-like calcification in the wall. In this report, we describe the contrast-enhanced spectral mammography (CESM), ultrasonography, and computed tomography findings and provide a reference for the diagnosis of EICs. To the best of our knowledge, this is the first report of the CESM findings of an EIC. Our case illustrates that CESM has excellent performance similar to that of magnetic resonance imaging and is much more effective than conventional digital mammography. Additionally, our case indicates that precise correlation of CESM with ultrasonography findings contributes to the diagnosis of EICs. This rare case with multiple imaging findings will increase the awareness of EICs in the breast parenchyma.


2016 ◽  
Vol 43 (2) ◽  
pp. 216-218 ◽  
Author(s):  
So-Min Hwang ◽  
Sang-Hwan Lee ◽  
Min-Wook Kim ◽  
Hwal-Woong Kim

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