Turcot syndrome and Gardner's syndrome in a female patient with familial colon adenomatosis. A case report and literature review

2019 ◽  
Vol 83 (6) ◽  
pp. 72
Author(s):  
A. M. Kuz'minov ◽  
D. V. Vyshegorodtsev ◽  
M. Kh. Toboeva ◽  
V. Yu. Korolik ◽  
A. V. Gavryushin ◽  
...  
2020 ◽  
Vol 10 (2) ◽  
pp. 47-52
Author(s):  
I. L. Chernikovskiy ◽  
D. N. Korobkov ◽  
N. V. Savanovich ◽  
D. A. Chernikov ◽  
P. V. Melnikov ◽  
...  

Gardner’s syndrome is a genetically determined disease characterized by a combination of colon polyposis, osteomas, and various soft tissue tumors. In this article, we discuss disease epidemiology, etiology, manifestations, and treatment methods. We also report a case of Gardner’s syndrome.


2020 ◽  
Author(s):  
Raffaele Vitiello ◽  
Tommaso Greco ◽  
Luigi Cianni ◽  
Silvia Careri ◽  
Maria Serena Oliva ◽  
...  

Osteoma is a benign, slowly growing, asymptomatic, bone-forming tumor arising from cancellous or compact bone. Osteoma usually is a solitary lesion, but in patients with Gardner’s Syndrome it may be multiple. osteoma may rarely have a parosteal localization. Parosteal osteoma has peculiar radiographic, histologic and clinical features. We describe a case report of a 51- years old man with a bifocal parosteal osteoma of the femur in a non-syndromic patient. This is the first described patient with a bifocal lesion. In literature only 24 cases of paraosteal osteoma are found. Our patient underwent surgery and the lesions were fully excised. At one year follow-up there was no evidence of recurrence.


2003 ◽  
Vol 44 (2) ◽  
pp. 158-159 ◽  
Author(s):  
K. Chelaifa ◽  
K. Bouzaidi ◽  
S. Chouaib ◽  
O. Azaiz ◽  
M. Ben Messaoud ◽  
...  

1986 ◽  
Vol 47 (12) ◽  
pp. 1628-1633
Author(s):  
Takashi HORIE ◽  
Haruhiko NAITO ◽  
Tsuyoshi TAKAHASHI ◽  
Kenji YAMAMOTO ◽  
Toshihiko TSUBURAYA ◽  
...  

2019 ◽  
Vol 11 (2) ◽  
pp. 180-186
Author(s):  
Monthanat Ploydaeng ◽  
Salinee Rojhirunsakool ◽  
Poonkiat Suchonwanit

Localized hypertrichosis with traumatic panniculitis is considered a rare condition. Previous articles have reported occurrence in females aged between 20 and 35 years. Possible mechanisms of trauma-induced localized hypertrichosis include hyperemia and angiogenesis induced by local inflammation, which can alter the hair growth cycle. The presence of inflammatory cells and lipomembranous changes on histopathology can support the diagnosis. We herein present a 35-year-old female patient with localized hypertrichosis following blunt trauma.


1998 ◽  
Vol 49 (3) ◽  
pp. 302-305 ◽  
Author(s):  
Jacques Noterman M.D., Ph.D. ◽  
Nicolas Massager M.D. ◽  
Michel Vloeberghs M.D. ◽  
Jacques Brotchi M.D., Ph.D.

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