Fibrous dysplasia associated with intramuscular myxoma (Mazabraud's syndrome): a long-term follow-up of three cases

1998 ◽  
Vol 124 (7) ◽  
pp. 401-406 ◽  
Author(s):  
Miklós Szendrói ◽  
Pál Rahóty ◽  
Imre Antal ◽  
János Kiss

1994 ◽  
Vol 73 (5) ◽  
pp. 328-330 ◽  
Author(s):  
Martin J. Donnelly ◽  
Donald P. McShane ◽  
Hugh Burns

Fibrous dysplasia of bone is a benign idiopathic disorder where abnormal fibro-osseous tissue replaces normal bone. The bony abnormalities may be associated with endocrine disorders and abnormal pigmentation of the skin and mucous membranes. Involvement of the temporal bone is a very rare occurrence. We report a case of monostotic fibrous dysplasia of the temporal bone with associated lymphadenopathy. To our knowledge this association has not been previously described in the literature. We also emphasise the need for long term follow up of patients with this condition as cholesteatoma may develop insidiously.



2021 ◽  
Author(s):  
João Victor Bezerra Ramos ◽  
João Lucas Pordeus de Menezes ◽  
Louyse Jerônimo de Morais ◽  
Maurus Marques de Almeida Holanda

Background: Fibrous dysplasia is a congenital and benign bone tumor. There may be malignant transformation in some cases, with a mortality rate of 53.6%. Objectives and Methods: To describe a patient with fibrous dysplasia in childhood in the parietal and temporal bones, and to report the importance of surgical correction to prevent malignant transformation. The case was studied and came from a referral hospital – João Pesssoa, PB. Results: History of daily headache and bulging in the temporal and parietal regions on the right. Computed tomography revealed lesions in the aspect of “ground glass”. Surgery was performed with exposure of two lesions, with craniectomy, followed by cranioplasty. Such an approach should be recommended, since malignant transformation occurs in up to 1% of cases, but after radiotherapy this rate can reach 44% of cases, mainly osteosarcoma. In this case, the anatomopathological study revealed a diagnosis of fibrous dysplasia and the patient has been followed up for 20 years without recurrences, which are common in adolescence. Conclusions: It is important to make a differential diagnosis with malignant diseases, in addition to contraindicating radiotherapy to prevent malignant transformation; long-term follow-up is essential to avoid relapses and / or complications resulting from the disease.



2017 ◽  
Vol 8 (1) ◽  
pp. 209 ◽  
Author(s):  
IanF Dunn ◽  
DavidL Penn ◽  
RichardJ Tartarini ◽  
CarolynH Glass ◽  
Umberto De Girolami ◽  
...  


2021 ◽  
Vol 34 (3) ◽  
pp. 226-230
Author(s):  
MAKI IZAWA ◽  
YUSEI OTAKA ◽  
NORIYOSHI SHIBA ◽  
NOBUTOSHI TAKAHASHI ◽  
TSUNEYASU TATSUTA ◽  
...  


1990 ◽  
Vol 36 (1) ◽  
pp. 177-183
Author(s):  
Masaru HATTORI ◽  
Yoshiki TAKAI ◽  
Toshiyasu YAMASHITA ◽  
Hidenori MATSUSHITA ◽  
Kazuhisa NAKAYAMA ◽  
...  


2019 ◽  
Vol 42 ◽  
Author(s):  
John P. A. Ioannidis

AbstractNeurobiology-based interventions for mental diseases and searches for useful biomarkers of treatment response have largely failed. Clinical trials should assess interventions related to environmental and social stressors, with long-term follow-up; social rather than biological endpoints; personalized outcomes; and suitable cluster, adaptive, and n-of-1 designs. Labor, education, financial, and other social/political decisions should be evaluated for their impacts on mental disease.



2001 ◽  
Vol 3 (1) ◽  
pp. 28-32 ◽  
Author(s):  
J. Tiainen ◽  
M. Matikainen ◽  
P. Aitola ◽  
K-M. Hiltunen ◽  
J. Mattila


2001 ◽  
Vol 120 (5) ◽  
pp. A397-A397
Author(s):  
M SAMERAMMAR ◽  
J CROFFIE ◽  
M PFEFFERKORN ◽  
S GUPTA ◽  
M CORKINS ◽  
...  


2001 ◽  
Vol 120 (5) ◽  
pp. A204-A204
Author(s):  
B GONZALEZCONDE ◽  
J VAZQUEZIGLESIAS ◽  
L LOPEZROSES ◽  
P ALONSOAGUIRRE ◽  
A LANCHO ◽  
...  


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