Review of current therapies for secondary hypertrophic pulmonary osteoarthropathy

被引:43
作者
Sheila Nguyen [3 ]
Hojjati, Mehrnaz [1 ,2 ]
机构
[1] Univ Minnesota, Med Rheumatol Off, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Div Rheumat & Autoimmune Dis, Dept Med, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Sch Med, Minneapolis, MN 55455 USA
关键词
Bisphosphonates; Gefetinib; Octreotide; Osteoarthropathy; Secondary hypertrophic; Therapy; Treatment; Vagotomy; OF-THE-LITERATURE; CONGENITAL HEART-DISEASE; MARIE-BAMBERGER-SYNDROME; LIVER-TRANSPLANTATION; CYSTIC-FIBROSIS; BRONCHOGENIC-CARCINOMA; RESISTANT PAIN; TUMOR RESPONSE; REVERSAL; LUNG;
D O I
10.1007/s10067-010-1563-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hypertrophic osteoarthropathy (HOA) is a disabling condition that may occur secondarily to primary lung cancer. It is characterized by digital clubbing, arthralgia/arthritis, and periostosis of the tubular bones. The pain associated with HOA can be disabling and often refractory to conventional analgesics. We performed a comprehensive review of the literature using the PubMed database on treatment modalities available for HOA. We found 52 relevant articles-40 case reports, six case series, two review papers, and four combined case series and review papers. There were no randomized controlled trials reported. We then classified treatments used for HOA into two categories: (1) treatment of primary cause (i.e., resection of tumor, chemotherapy, radiotherapy, treatment of infection, etc.) and (2) symptomatic treatments (i.e., bisphosphonates, octreotide, NSAIDs, vagotomy, etc.). Subsequently, we summarized the main findings for each treatment. Although the clinical diagnosis of HOA has existed for over 100 years, the pathogenesis mechanism has not yet been elucidated, and treatment options for this condition remain experimental. Primary treatment is the most widely reported modality to be efficacious. In cases which primary therapy is not possible, several symptomatic treatment modalities are suggested, with various degree of success. Further research is needed to clarify the pathophysiological mechanism of HOA as to appropriately direct therapy.
引用
收藏
页码:7 / 13
页数:7
相关论文
共 67 条
  • [1] Akizuki M, 1991, Ryumachi, V31, P311
  • [2] AKIZUKI M, 1991, RYUMACHI, V31, P316
  • [3] Postchemotherapeutic reversibility of hypertrophic osteoarthropathy in a patient with bronchogenic adenocarcinoma
    Albrecht, S
    Keller, A
    [J]. CLINICAL NUCLEAR MEDICINE, 2003, 28 (06) : 463 - 466
  • [4] Hypertrophic osteoarthropathy secondary to vascular prosthesis infection -: Report of 3 cases and review of the literature
    Alonso-Bartolome, Pilar
    Martinez-Taboada, Victor Manuel
    Pina, Trinitario
    Blanco, Ricardo
    Rodriguez-Valverde, Vicente
    [J]. MEDICINE, 2006, 85 (03) : 183 - 191
  • [5] Hypertrophic pulmonary osteoarthropathy: control of pain and symptoms with pamidronate
    Amital, H
    Applbaum, YH
    Vasiliev, L
    Rubinow, A
    [J]. CLINICAL RHEUMATOLOGY, 2004, 23 (04) : 330 - 332
  • [6] Hypertrophic pulmonary osteoarthropathy (HPOA) (Pierre Marie-Bamberger syndrome): two cases presenting as acute inflammatory arthritis. Description and review of the literature
    Armstrong, David J.
    McCausland, Elisabeth M. A.
    Wright, Gary D.
    [J]. RHEUMATOLOGY INTERNATIONAL, 2007, 27 (04) : 399 - 402
  • [7] ATKINSON MK, 1976, CANCER-AM CANCER SOC, V38, P1729, DOI 10.1002/1097-0142(197610)38:4<1729::AID-CNCR2820380446>3.0.CO
  • [8] 2-#
  • [9] Vascular endothelial growth factor (VEGF)-A and platelet-derived growth factor (PDGF) play a central role in the pathogenesis of digital clubbing
    Atkinson, S
    Fox, SB
    [J]. JOURNAL OF PATHOLOGY, 2004, 203 (02) : 721 - 728
  • [10] Reversal of digital clubbing after lung transplantation in cystic fibrosis patients: A clue to the pathogenesis of clubbing
    Augarten, A
    Goldman, R
    Laufer, J
    Szeinberg, A
    Efrati, O
    Barak, A
    Miller, MS
    Yahav, Y
    [J]. PEDIATRIC PULMONOLOGY, 2002, 34 (05) : 378 - 380