==== Front Ann Saudi MedAnn Saudi MedAnnals of Saudi Medicine0256-49470975-4466King Faisal Specialist Hospital and Research Centre 10.5144/0256-4947.2006.489asm-6-489What's Your Diagnosis?DIAGNOSIS: Hypertrophic pulmonary osteoarthropathy due to carcinoma of the right lung Parameswaran Bimal Al Dossary Jamila Salmaniya Medical Complex, Manama, BahrainCorrespondence and reprint requests: Bimal Kumar Parameswaran, MD, Department of Radiology, Salmaniya Medical Complex, Manama, Bahrain, T: +973-1-728 9008, F: +973-1-728 9030, drbimalkumar@yahoo.comNov-Dec 2006 26 6 489 491 Copyright © 2006, Annals of Saudi Medicine2006This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. ==== Body The radiograph of the knees (Figure 1) shows periosteal thickening at the metadiaphysis of the distal femur and proximal tibia and fibula on both sides. The knee joint space is maintained and there are no periarticular erosions. The radiograph of ankles (Figure 2) reveals a similar periosteal reaction in the distal tibia and fibula, which is most conspicuous along the dorsal aspect with a normal appearance of the joints. The differential diagnosis for this pattern of bilateral periosteal reaction includes hypertrophic pulmonary osteoarthropathy (HOA), pachydermoperiostosis, thyroid acropachy and vascular insufficiency. The chest radiograph (Figure 3) reveals a mass without air bronchogram in the right paracardiac region and right pleural effusion. CT of the chest (Figure 4) shows the mass as a lobulated lesion in the right middle and lower lobe abutting the mediastinum associated with right pleural effusion. The features in chest imaging are those of a lung carcinoma. The combination of all radiological findings leads us to the diagnosis of hypertrophic pulmonary osteoarthropathy (HOA) due to carcinoma of the right lung. Biopsy of the lung mass revealed the lesion to be a moderately differentiated adenocarcinoma. Discussion HOA is a syndrome charecterized by digital clubbing and periostosis of the tubular bones.1 The syndrome occurs in two forms—primary and secondary. The primary form, also termed pachydermoperiostosis, is an autosomal dominant condition characterized by coarsening of facial features, mild bone and joint involvement and early onset of disease, usually in the second decade of life. Secondary HOA occurs mostly in adults and is associated with an underlying disease, usually an intrathoracic malignancy or infection.2 Pulmonary causes for HOA include bronchogenic carcinoma, pleural mesothelioma, chronic bronchitis, bronchiectasis, pulmonary fibrosis, and pneumoconiosis. Though the syndrome was originally referred to as pulmonary hypertrophic osteoarthropathy, the term “hypertrophic osteoarthropathy” is becoming more common as there are many extrapulmonary diseases that cause HOA. These include cardiovascular diseases like cyanotic congenital heart disease, bacterial endocarditis and aortic aneurysm; gastrointestinal diseases like inflammatory bowel disease, Whipple’s disease, gastrointestinal tract malignancies and amebic dysentery; hepatobiliary diseases, thyroid acropachy, acquired immune deficiency syndrome, cystic fibrosis and sarcoidosis.2 HOA may be associated with any cell type of lung cancer, most frequently with squamous and adenocarcinoma and least frequently with small cell lung carcinoma.3 In our patient, biopsy of the lung tumor revealed it to be a well differentiated adenocarcinoma. Hypertrophic osteoarthropathy may affect up to 10% of patients with adenocarcinoma of the lung.4 Clinically, HOA presents as clubbing of the digits, oligoarthritis or polyarthritis of the distal joints, tender periostitis of the distal long bones, and noninflammatory synovial effusions.4 Positive laboratory findings in HOA include an elevated erythrocyte sedimentation rate and if there is considerable new bone formation, elevated serum alkaline phosphatase. Rheumatoid factor and antinuclear antibody are negative.2 The exact etiology of HOA is unknown. Roles have been proposed for reflex vagal stimulation, growth factors, hormonal and immune mechanisms.2 It has been suggested that vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF) released after platelet clusters impact in the distal vasculature may induce the stromal and vascular changes present in digital clubbing.5 The primary and secondary types of HOA display similar radiographic changes.6 The radiographic findings of HOA may occur in the absence of any clinical findings, and uncommonly, radiographs are normal in the presence of florid clinical disease.2 Periosteal proliferation is the hallmark of HOA.7 Changes are most often seen in the tibia, radius, ulna, fibula, and femur.2 The short and flat bones are involved in about 18.5% of patients and show less pronounced periosteal reaction than in the long bones.8 A three-dimensional pattern of evolution of periostosis has been described in HOA, with the three dimensions being (1) the number of bones affected (2) the area of involvement of a given bone and (3) the shape of the periostosis. In early and mild cases few bones are affected and the periosteal bone apposition is limited to the diaphysis with a monolayer configuration. Advanced cases are characterized by involvement of practically all tubular bones with an irregular periosteal reaction that extends to involve the metaphysis and even the epiphysis. The adjacent joints characteristically do not show any narrowing of the joint space, in particular osteoporosis or erosions.7 Radiographic changes described in the terminal phalanges include osteolysis with truncation, overgrowth with mushrooming of the tuft and tapering of the bones.7 In our patient, advanced changes of periostosis were seen in the leg bones while the forearm bones showed mild involvement. Radionuclear scans are more sensitive than radiographs and reveal the bone involvement by HOA at an earlier stage.9 Radionuclide scintigraphy shows diffuse symmetrical increased uptake along the cortical margins of the diaphysis of the involved bones, referred to as the ‘tramline sign’, ‘parallel tract sign’ or ‘double stripe’ sign.10,11 Associated synovitis may produce increased uptake in juxta-articular bone and increased uptake is also seen in the distal phalanges affected with marked clubbing.11 Magnetic resonance imaging (MRI) of patients with HOA shows, in addition to the periosteal reaction, significant soft tissue changes, which are not well appreciated with other diagnostic modalities. The soft tissue changes depicted with MRI are extensive swelling in the tissues surrounding the bone without involving the bone itself and muscular and preseptal edema, all seen as hyperintense signal in T2-weighted images.12 When newly discovered, the presence of clubbing, with or without HOA, warrants a chest roentgenogram to look for a pulmonary neoplasm, which may still be localized and therefore curable. If the plain film is unrevealing, a CT scan of the thorax is indicated.13 The most effective treatment for the pain and discomfort of secondary HOA is cure of the underlying condition. Tumor ablation or chemosuppressive therapy of an associated malignancy often results in prompt reversal of symptoms and resolution or disappearance of the radiographic and radionuclide imaging findings.2,11 Figure 1 Radiograph of the knees showing irregular periosteal thickening of the metadiaphysis of the tibia, fibula and femur bilaterally, which is most marked in the femora. Figure 2 Radiograph of the ankles showing a periosteal reaction, especially along the dorsal aspect of the tibia and fibula. Figure 3 Chest radiograph showing right lung mass and pleural effusion. Figure 4 CT of the chest showing lobulated mass in the right middle lobe abutting the mediastinum and right pleural effusion. ==== Refs References 1 Martinez-Lavin M Matucci-Cerinic M Jajic I Pineda C Hypertrophic osteoarthropathy. Consensus on its definition, classification, assessment and diagnostic criteria J Rheumatol 1993 20 1386 1387 7901413 2 Altman RD Tenenbaum J Hypertrophic osteoarthropathy Harris ED Jr Budd RC Genovese MC Firestein GS Sargent JS Sledge SB Kelley’s Textbook of Rheumatology 7th ed Elsevier Saunders Philadelphia 2005 1748 52 3 Beckles MA Spiro SG Colice GL Rudd RM The physiologic evaluation of patients with lung cancer being considered for resectional surgery Chest 2003 123 1 105S 114S 12527570 4 Rugo HS Paraneoplastic syndromes and other non-neoplastic effects of cancer Goldman L Ausiello D Cecil Textbook of Medicine 22 nd edition 2004 WB Saunders 1129 5 Atkinson S Fox SB Vascular endothelial growth factor (VEGF)-A and platelet-derived growth factor (PDGF) play a central role in the pathogenesis of digital clubbing J Pathol 2004 203 2 721 8 15141388 6 Pineda CJ Martinez-Lavin M Goober JE Sartris DJ Clopton P Resnick D Periostitis in hypertrophic osteoarthropathy: relationship to disease duration Am J Roentgenol 1987 148 773 8 3493663 7 Pineda C Fonesca C Martinez-Lavin M The spectrum of soft tissue and skeletal abnormalities of hypertrophic osteoarthropathy J Rheumatol 1990 17 5 626 32 2359073 8 Jajic Z Jajic I Radiological changes of short and flat bones in primary hypertrophic osteoarthropathy Ann Rheum Dis 1998 57 747 748 10070276 9 Lopez-Majano V Sobti P Early diagnosis of pulmonary osteoarthropathy in neoplastic disease J Nucl Med Allied Sci 1984 28 69 76 6239914 10 Love C Din AS Tomas MB Kalapparambath TP Palestro CJ Radionuclide Bone Imaging: An Illustrative Review Radiographics 2003 23 341 358 12640151 11 Rosenthal L Kirsch J Observation of radionuclide imaging in hypertrophic pulmonary osteoarthropathy Radiology 1976 120 359 362 935484 12 Capelastegui A Astigarraga E Garcia-Iturraspe C MR findings in pulmonary hypertrophic osteoarthropathy Clin Rad 2000 55 1 72 75 13 Murray FJ History and Physical Examination Murray FJ Nadel JA Textbook of Respiratory Medicine 3 rd edition WB Saunders 2000 601