Literature DB >> 17539760

Orthopaedic manifestations of Gaucher disease.

Kevin F Lutsky1, Nirmal C Tejwani.   

Abstract

Gaucher disease is a rare, hereditary disease caused by lack of a lysosomal enzyme. This results in the accumulation of glucocerebroside in the cells of the reticuloendothelial system, including the bone marrow. The orthopaedic manifestations of this disease are important for the orthopaedic surgeon to recognize and understand. Patients with Gaucher disease are at risk for pathologic fracture, abnormal bony remodeling and delayed healing, increased intraoperative bleeding, and infection. Osteomyelitis and avascular necrosis, two common sequelae of the disease, can present in very similar fashions and warrant careful and accurate diagnosis to ensure proper treatment. The impact of Gaucher disease on the musculoskeletal system is reviewed with emphasis on the importance of understanding these effects for the treating orthopaedic surgeon.

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Year:  2007        PMID: 17539760

Source DB:  PubMed          Journal:  Bull NYU Hosp Jt Dis        ISSN: 1936-9719


  7 in total

1.  Gaucher disease with pathological femoral neck fracture.

Authors:  Emine Binnetoglu; Erkam Komurcu; Hacer Sen; Betul Kizildag
Journal:  BMJ Case Rep       Date:  2013-08-30

2.  Bone marrow involvement in Gaucher disease at MRI : what long-term evolution can we expect under enzyme replacement therapy?

Authors:  Benjamin Fedida; Sébastien Touraine; Jerôme Stirnemann; Nadia Belmatoug; Jean-Denis Laredo; David Petrover
Journal:  Eur Radiol       Date:  2015-04-16       Impact factor: 5.315

3.  Extraosseous extension caused by epidural hematoma in Gaucher disease mimicking malignant bone tumor.

Authors:  Tadahiko Kubo; Shoji Shimose; Jun Fujimori; Ryo Shimizu; Mitsuo Ochi
Journal:  JIMD Rep       Date:  2013-12-21

Review 4.  An overview on bone manifestations in Gaucher disease.

Authors:  Peter Mikosch; Derralynn Hughes
Journal:  Wien Med Wochenschr       Date:  2010-12

Review 5.  Gaucher disease - more than just a rare lipid storage disease.

Authors:  Jaehyeok Roh; Subbaya Subramanian; Neal J Weinreb; Reena V Kartha
Journal:  J Mol Med (Berl)       Date:  2022-01-23       Impact factor: 4.599

6.  Splenomegaly as a primary manifestation of Gaucher disease in a young adult woman.

Authors:  Giuseppe Merra; Antonio Dal Lago; Roberta Ricci; Daniela Antuzzi; Giovanni Gasbarrini; Antonio Gasbarrini; Giovanni Ghirlanda
Journal:  Case Rep Gastroenterol       Date:  2008-11-29

7.  Lysosomal Storage Disorders: Clinical, Biochemical and molecular profile from Rare disease centre, India.

Authors:  Manisha Goyal; Ashok Gupta
Journal:  Ann Indian Acad Neurol       Date:  2021-03-27       Impact factor: 1.383

  7 in total

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