scholarly journals Sclerosing Bone Dysplasia from 16th Century Sardinia (Italy): A Possible Case of Camurati-Engelmann Disease

2016 ◽  
Vol 26 (5) ◽  
pp. 830-841 ◽  
Author(s):  
V. Giuffra ◽  
A. Montella ◽  
R. Bianucci ◽  
M. Milanese ◽  
E. Tognotti ◽  
...  
Keyword(s):  
Bone Dysplasia ◽  
16Th Century ◽  
Sclerosing Bone Dysplasia ◽  
Engelmann Disease

scholarly journals Correction of Orbital Deformity in Camurati-Engelmann Disease with PEEK Lateral Wall Implants

2021 ◽  
Vol 6 ◽  
pp. 247275122110091
Author(s):  
Thomas E. Howe ◽  
Damithri T. Goonesekera ◽  
Nicolas J. Lee ◽  
Sachin M. Salvi
Keyword(s):  
Skull Base ◽  
Bone Dysplasia ◽  
Lateral Wall ◽  
Cutting Edge ◽  
Patient Specific ◽  
The Novel ◽  
Facial Profile ◽  
Sclerosing Bone Dysplasia ◽  
Orbital Wall ◽  
Engelmann Disease

Camurati-Engelmann Disease is a rare congenital sclerosing bone dysplasia condition. Affected patients manifest bony abnormalities including thickening of the skull base and orbital bones. The resulting orbital volume reduction associated with this condition can cause exophthalmos, distorting the facial profile. The authors report a 33-year-old man with a diagnosis of Camurati-Engelmann Disease exhibiting exophthalmos who was successfully treated with the insertion of bilateral lateral orbital wall patient specific PEEK implants via a bi-coronal flap approach. This case highlights the novel application of modern cutting-edge technology in the treatment of proptosis in Camurati-Engelmann Disease.

Mixed sclerosing bone dysplasia—a case report with literature review

2003 ◽  
Vol 27 (3) ◽  
pp. 203-205 ◽  
Author(s):  
Sandeep Ghai ◽  
Raju Sharma ◽  
Sangeet Ghai
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Bone Dysplasia ◽  
Sclerosing Bone Dysplasia

Melorheostosis: a rare sclerosing bone dysplasia. Usefulness of bone scintigraphy

2019 ◽  
Vol 38 (4) ◽  
pp. 243-244
Author(s):  
E.R. Marqués Aparicio ◽  
J. Dolado Ardit ◽  
A. Crespo-Jara ◽  
A. Martínez Caballero ◽  
M.A. Antón Leal ◽  
...  
Keyword(s):  
Bone Scintigraphy ◽  
Bone Dysplasia ◽  
Sclerosing Bone Dysplasia

Exome sequencing reveals a mutation in DMP1 in a family with familial sclerosing bone dysplasia

Bone ◽  
2014 ◽  
Vol 68 ◽  
pp. 142-145 ◽  
Author(s):  
Marie-Hélène Gannagé-Yared ◽  
Periklis Makrythanasis ◽  
Eliane Chouery ◽  
Cristina Sobacchi ◽  
Cybel Mehawej ◽  
...  
Keyword(s):  
Exome Sequencing ◽  
Bone Dysplasia ◽  
Sclerosing Bone Dysplasia

Mesenteric Fibromatosis in a Patient with Camurati-Engelmann Disease. A Case Report and Literature Review

2005 ◽  
Vol 91 (6) ◽  
pp. 552-554 ◽  
Author(s):  
Pierluigi Ballardini ◽  
Loretta Gulmini ◽  
Guido Margutti ◽  
Giorgio Lelli
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Diseases ◽  
Bone Dysplasia ◽  
Low Grade ◽  
Long Bones ◽  
Rare Form ◽  
Rare Type ◽  
Mesenteric Fibromatosis ◽  
Engelmann Disease

Mesenteric fibromatosis is a rare type of desmoid tumor characterized by local aggressiveness and a tendency to relapse. In view of these characteristics it may be considered a low-grade fibrosarcoma. Camurati-Engelmann disease is a very rare form of bone dysplasia characterized by osteosclerosis of the diaphyses of the long bones. Here we describe the case of a male patient affected by these two rare diseases in association with chronic inflammatory intestinal disease.

Melorheostosis: a Rare Sclerosing Bone Dysplasia

2017 ◽  
Vol 15 (4) ◽  
pp. 335-342 ◽  
Author(s):  
Anupam Kotwal ◽  
Bart L. Clarke
Keyword(s):  
Bone Dysplasia ◽  
Sclerosing Bone Dysplasia

Sclerosing Bone Dysplasia

Orthopedics ◽  
1981 ◽  
Vol 4 (1) ◽  
pp. 100-100
Author(s):  
Wilton H Bunch
Keyword(s):  
Bone Dysplasia ◽  
Sclerosing Bone Dysplasia

scholarly journals A new familial sclerosing bone dysplasia

2010 ◽  
Vol 25 (3) ◽  
pp. 676-680 ◽  
Author(s):  
Eliane Chouery ◽  
Alessandra Pangrazio ◽  
Annalisa Frattini ◽  
Anna Villa ◽  
Liesbeth Van Wesenbeeck ◽  
...  
Keyword(s):  
Bone Dysplasia ◽  
Sclerosing Bone Dysplasia

scholarly journals Sclerosteosis: A Rare, Sclerosing Bone Dysplasia in a Bangladeshi Male

2019 ◽  
Vol 1 (2) ◽  
pp. 35-40
Author(s):  
Shahed Morshed ◽  
Keyword(s):  
Clinical Features ◽  
Multidisciplinary Team ◽  
Bone Dysplasia ◽  
Team Approach ◽  
Separate Entity ◽  
Multidisciplinary Team Approach ◽  
Sclerosing Bone Dysplasia

We report a 26-year-old male who was initially diagnosed as osteopetrosis and referred for endocrine evaluations. But due to specific clinical features supported by investigations, we diagnosed the case as sclerosteosis. The patient was managed by a multidisciplinary team approach. Sclerosteosis may be erroneously diagnosed as osteopetrosis. However, many unique features make it a separate entity.

Sign in / Sign up

Export Citation Format

Share Document