A rare case of pediatric linear syringocystadenoma papilliferum of the chest

2021 ◽  
Vol 73 (5) ◽  
Author(s):  
Mattia GIOVANNINI ◽  
Teresa ORANGES ◽  
Francesca PORTELLI ◽  
Andrea BASSI ◽  
Fausto A. PEDACI ◽  
...  
2018 ◽  
pp. 33-38 ◽  
Author(s):  
Payal Chauhan ◽  
Rishabh Kumar Chauhan ◽  
Amrita Upadhyaya ◽  
Sanjeev Kishore

2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
Megumi Nishioka ◽  
Atsushi Tanemura ◽  
Takashi Yamanaka ◽  
Noriko Umegaki ◽  
Mamori Tani ◽  
...  

We report a rare case of giant squamous cell carcinoma of the buttock infiltrated to the rectum. The tumor may have arisen from syringocystadenoma papilliferum. Since there was no sign of metastasis, radical operation including rectal amputation was performed after successful neoadjuvant therapies. Afterwards, the patient has been alive free from disease for 15 months with no lymph node and distant organ metastasis.


2021 ◽  
pp. 85-86
Author(s):  
Naveen K ◽  
Ganesan M

Syringocystadenoma papilliferum is a rare benign adnexal tumor of apocrine or eccrine glands. It is a childhood tumor with a relatively higher incidence at birth. The common sites of occurrence are the face and scalp. The propensity of the nodular lesion is towards the trunk, but here in our case, we present a case of nodular syringocystadenoma papilliferum of the scalp. The tumor can arise de novo or from pre-existing naevus sebaceous. The tumor rarely has a malignant course, most often basal cell carcinoma. Herein, we present an adolescent with the nodular type of syringocystadenoma papilliferum of the scalp, treated with surgical excision.


2019 ◽  
Vol 35 (2) ◽  
pp. 151-154
Author(s):  
Yaşar Subutay Peker ◽  
Murat Urkan ◽  
Salih Hamcan ◽  
Ali Fuat Çiçek ◽  
Mehmet Ali Gülçelik

2016 ◽  
Vol 43 (2) ◽  
pp. 96
Author(s):  
PrasmitAmit Shah ◽  
VikasShyamraj Singh ◽  
Surekha Bhalekar ◽  
S Sudhamani ◽  
Ekta Paramjit

Author(s):  
S. K. Peng ◽  
M.A. Egy ◽  
J. K. Singh ◽  
M.B. Bishop

Electron microscopy and energy dispersive x-ray microanalysis (EDXA) are found to be very useful tools for identification of etiologic agents in pneumoconiosis or interstitial pulmonary disorders. Pulmonary interstitial fibrosis and granulomatosis are frequently associated with occupational and environmental pollution. Numerous reports of pneumoconiosis in various occupations such as coal and gold miners are presented in the literature. However, there is no known documented case of pulmonary changes in workers in the sandpaper industry. This study reports a rare case of pulmonary granulomatosis containing deposits from abrasives of sandpaper diagnosed by using EDXA.


2015 ◽  
Vol 21 ◽  
pp. 143
Author(s):  
Elizabeth Sanchez Rangel ◽  
Maria Moscoso Cordero ◽  
Vinuta Mohan ◽  
Tasneem Zahra

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