Literature DB >> 27582999

Primum non nocere: a case of a humeral fracture in a patient with fibrodysplasia progressiva ossificans.

Alun Yewlett1, Jeff Kitson1, Andrew Redfern2, Chris Smith1.   

Abstract

Fibrodysplasia progressiva ossificans (FPO) is an extremely rare condition characterized by abnormal heterotopic bone formation. The condition is eponymously known as 'stoneman' disease because patients can become effectively entombed within abnormal heterotopic bone. We present the first known case of a diaphyseal humeral fracture managed conservatively in an adult patient with this condition. This patient already had a pre-existing bony bar from a fusion mass involving the thoracic spine, scapula and ribs to her proximal humerus splinting the arm in a position of adduction with the palm of her hand facing towards her groin. This patient also suffered a concomitant unstable cervical spinal fracture for which full spinal precautions were needed. As a result of the rapid bone forming nature of her condition, the humeral fracture was placed in a position where the hand would face outwards to make perineal care and personal hygiene easier in that the fracture was expected to unite in this new position as a result of her FPO.

Entities:  

Keywords:  case report; conservative treatment; fibrodysplasia progressiva ossificans; humeral fracture

Year:  2015        PMID: 27582999      PMCID: PMC4935172          DOI: 10.1177/1758573215598498

Source DB:  PubMed          Journal:  Shoulder Elbow        ISSN: 1758-5732


  7 in total

1.  A Tumour for which Surgery will do more harm than good: A Case Report of Fibrodysplasia Ossificans Progressiva.

Authors:  H A Obamuyide; S O Ogunlade
Journal:  Niger Postgrad Med J       Date:  2015-03

2.  Anaesthesia in myositis ossificans progressiva. A case report and clinical review.

Authors:  E A Shipton; L W Retief; H D Theron; F A de Bruin
Journal:  S Afr Med J       Date:  1985-01-05

Review 3.  Fibrodysplasia ossificans progressiva: clinical course, genetic mutations and genotype-phenotype correlation.

Authors:  Irina Hüning; Gabriele Gillessen-Kaesbach
Journal:  Mol Syndromol       Date:  2014-08-07

4.  Early mortality and cardiorespiratory failure in patients with fibrodysplasia ossificans progressiva.

Authors:  Frederick S Kaplan; Michael A Zasloff; Joseph A Kitterman; Eileen M Shore; Charles C Hong; David M Rocke
Journal:  J Bone Joint Surg Am       Date:  2010-03       Impact factor: 5.284

5.  Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva.

Authors:  Joseph A Kitterman; Sharon Kantanie; David M Rocke; Frederick S Kaplan
Journal:  Pediatrics       Date:  2005-10-17       Impact factor: 7.124

6.  Fibrodysplasia ossificans progressiva. The clinical features and natural history of 34 patients.

Authors:  J M Connor; D A Evans
Journal:  J Bone Joint Surg Br       Date:  1982

Review 7.  Fibrodysplasia ossificans progressiva.

Authors:  Frederick S Kaplan; Martine Le Merrer; David L Glaser; Robert J Pignolo; Robert E Goldsby; Joseph A Kitterman; Jay Groppe; Eileen M Shore
Journal:  Best Pract Res Clin Rheumatol       Date:  2008-03       Impact factor: 4.098

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.