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Fibrous dysplasia & McCune-Albright syndrome: An experience from a tertiary care centre in north India
BACKGROUND & OBJECTIVES: Fibrous dysplasia (FD) is a rare metabolic bone disease and information available from India is limited to only anecdotal case reports. We describe the clinical profile and therapeutic outcome of 25 patients with FD observed over a period of 14 yr in a tertiary care cent...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121281/ https://www.ncbi.nlm.nih.gov/pubmed/21623035 |
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author | Bhadada, Sanjay Kumar Bhansali, Anil Das, Sambit Singh, Ramanbir Sen, R. Agarwal, A. Mittal, B.R. Nahar, Uma Dutta, Pinaki Khandelwal, Niranjan |
author_facet | Bhadada, Sanjay Kumar Bhansali, Anil Das, Sambit Singh, Ramanbir Sen, R. Agarwal, A. Mittal, B.R. Nahar, Uma Dutta, Pinaki Khandelwal, Niranjan |
author_sort | Bhadada, Sanjay Kumar |
collection | PubMed |
description | BACKGROUND & OBJECTIVES: Fibrous dysplasia (FD) is a rare metabolic bone disease and information available from India is limited to only anecdotal case reports. We describe the clinical profile and therapeutic outcome of 25 patients with FD observed over a period of 14 yr in a tertiary care centre from north India. METHODS: In this retrospective study patients (n = 25) with diagnosis of fibrous dysplasia based on either classical radiological features and/or histological evidence on bone biopsy, were analyzed. Associated endocrinopathies if any, were evaluated. The diagnosis of McCune Albright syndrome (MAS) was considered when fibrous dysplasia was accompanied by either café-au-lait macules and/or endocrinopathies. The clinical presentation, biochemical parameters and imaging were analysed. Seven patients received bisphosphonate therapy. The final outcome and side effects were noted. RESULTS: Age of the patients ranged from 7 to 48 yr (mean ± SD, 24.2 ± 11.4 yr) with a lag time between onset of symptoms and presentation ranging from 1 to 20 yr (mean ± SD, 6.6 ± 6.2 yr). The mean duration of follow up was 3.5 ± 2.1 yr. Eighteen (72%) patients had polyostotic disease while the remaining had monostotic FD. Eight patients had endocrinopathies: five had acromegaly, one each had gonadotropin independent precocious puberty (GIPP), hyperthyroidism and hypophosphatemic rickets. One child with GIPP later developed hyperthyroidism. McCune Albright syndrome was observed in 10 (40%) patients. A majority of the patients underwent various minor or major surgical procedures and seven patients received bisphosphonates for recurrent pathological fractures. Bone pain was reduced in all bisphosphonate treated patients with a decrease in subsequent fractures. INTERPRETATION & CONCLUSIONS: This series of FD patients from north India shows the varying presentations of this rare disease. Medical treatment with bisphosphonates appears to be potentially rewarding. |
format | Online Article Text |
id | pubmed-3121281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-31212812011-07-01 Fibrous dysplasia & McCune-Albright syndrome: An experience from a tertiary care centre in north India Bhadada, Sanjay Kumar Bhansali, Anil Das, Sambit Singh, Ramanbir Sen, R. Agarwal, A. Mittal, B.R. Nahar, Uma Dutta, Pinaki Khandelwal, Niranjan Indian J Med Res Original Article BACKGROUND & OBJECTIVES: Fibrous dysplasia (FD) is a rare metabolic bone disease and information available from India is limited to only anecdotal case reports. We describe the clinical profile and therapeutic outcome of 25 patients with FD observed over a period of 14 yr in a tertiary care centre from north India. METHODS: In this retrospective study patients (n = 25) with diagnosis of fibrous dysplasia based on either classical radiological features and/or histological evidence on bone biopsy, were analyzed. Associated endocrinopathies if any, were evaluated. The diagnosis of McCune Albright syndrome (MAS) was considered when fibrous dysplasia was accompanied by either café-au-lait macules and/or endocrinopathies. The clinical presentation, biochemical parameters and imaging were analysed. Seven patients received bisphosphonate therapy. The final outcome and side effects were noted. RESULTS: Age of the patients ranged from 7 to 48 yr (mean ± SD, 24.2 ± 11.4 yr) with a lag time between onset of symptoms and presentation ranging from 1 to 20 yr (mean ± SD, 6.6 ± 6.2 yr). The mean duration of follow up was 3.5 ± 2.1 yr. Eighteen (72%) patients had polyostotic disease while the remaining had monostotic FD. Eight patients had endocrinopathies: five had acromegaly, one each had gonadotropin independent precocious puberty (GIPP), hyperthyroidism and hypophosphatemic rickets. One child with GIPP later developed hyperthyroidism. McCune Albright syndrome was observed in 10 (40%) patients. A majority of the patients underwent various minor or major surgical procedures and seven patients received bisphosphonates for recurrent pathological fractures. Bone pain was reduced in all bisphosphonate treated patients with a decrease in subsequent fractures. INTERPRETATION & CONCLUSIONS: This series of FD patients from north India shows the varying presentations of this rare disease. Medical treatment with bisphosphonates appears to be potentially rewarding. Medknow Publications 2011-05 /pmc/articles/PMC3121281/ /pubmed/21623035 Text en © The Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Bhadada, Sanjay Kumar Bhansali, Anil Das, Sambit Singh, Ramanbir Sen, R. Agarwal, A. Mittal, B.R. Nahar, Uma Dutta, Pinaki Khandelwal, Niranjan Fibrous dysplasia & McCune-Albright syndrome: An experience from a tertiary care centre in north India |
title | Fibrous dysplasia & McCune-Albright syndrome: An experience from a tertiary care centre in north India |
title_full | Fibrous dysplasia & McCune-Albright syndrome: An experience from a tertiary care centre in north India |
title_fullStr | Fibrous dysplasia & McCune-Albright syndrome: An experience from a tertiary care centre in north India |
title_full_unstemmed | Fibrous dysplasia & McCune-Albright syndrome: An experience from a tertiary care centre in north India |
title_short | Fibrous dysplasia & McCune-Albright syndrome: An experience from a tertiary care centre in north India |
title_sort | fibrous dysplasia & mccune-albright syndrome: an experience from a tertiary care centre in north india |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121281/ https://www.ncbi.nlm.nih.gov/pubmed/21623035 |
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