scholarly journals Bifocal parosteal osteoma of femur: A case report and review of literature

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.

2012 ◽  
Vol 01 (01) ◽  
pp. 43-47 ◽  
Author(s):  
Sachin B. Punatar ◽  
Vanita Noronha ◽  
Amit Joshi ◽  
Kumar Prabhash

AbstractGardner′s syndrome is a variant of familial adenomatous polyposis. A multitude of extra-colonic manifestations including various endocrine tumors have been associated with this syndrome, the commonest of which is thyroid cancer. Majority of the patients with thyroid cancer and Gardner′s syndrome are females. Here we describe a male patient with Gardner′s syndrome who subsequently developed thyroid cancer.


2010 ◽  
Vol 22 ◽  
pp. 151-155
Author(s):  
Arati Chaudhary ◽  
PV Wanzari ◽  
Tushar Phulambrikar ◽  
Vanaja Reddy ◽  
Ashish Warhekar ◽  
...  

1981 ◽  
Vol 67 (3) ◽  
pp. 165-168
Author(s):  
J. V. Holland

AbstractA patient suffering from Gardner’s Syndrome is presented. The clinical features are described and the importance of early diagnosis discussed.


Author(s):  
Maria Eduarda Baldino ◽  
Valesca Sander Koth ◽  
Maria Noel Marzano Rodrigues Petruzzi ◽  
Fernanda Salum ◽  
Maria Antonia Figueiredo ◽  
...  

2018 ◽  
Vol 07 (11) ◽  
pp. 533-540
Author(s):  
Olfa Zoukar ◽  
Amel Khaskhoussy ◽  
Sonia Hammami ◽  
Sandra Zribi ◽  
Awatef Hajjajji ◽  
...  

2021 ◽  
pp. 112067212199767
Author(s):  
Iva Krolo ◽  
Aida Kasumović ◽  
Ivana Radman ◽  
Pavao Pavić

Purpose: Ocular features of Alport syndrome include anterior lenticonus, posterior polymorphous corneal dystrophy, and fleck-and-dot retinopathy in most cases. Keratoconus in such patients has been rarely mentioned in previous studies. To our knowledge, this is the first report of corneal cross-linking for halting the progression of keratoconus in a patient with Alport syndrome. Case report: A 22-year-old male was referred for his initial corneal topography, after he was already prescribed with rigid gas-permeable contact lenses. Alport syndrome was diagnosed in his infancy and gene COL4A5 mutation was confirmed. Ophthalmological evaluation confirmed keratoconus. One-year follow-up showed a progression on his right eye and standard corneal cross-linking was performed. Stabilization of the disease marked by normalization in visual function and corneal tomography values was noticed 1 year after the procedure. Conclusions: When diagnosing ocular clinical findings of Alport syndrome, keratoconus should be considered. Standard corneal cross-linking protocol can halt its progression.


2017 ◽  
Vol 23 (4) ◽  
pp. e9-e13
Author(s):  
S.A. Lalé ◽  
E.B. Burger ◽  
J.H.J.M. Bessems ◽  
V. Pollet ◽  
C.A. van Nieuwenhoven

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