This article has Open Peer Review reports available.
Massive hemoptysis and deep venous thrombosis presenting in a woman with Hughes-Stovin syndrome: a case report
© Al-Jahdali; licensee BioMed Central Ltd. 2010
Received: 13 January 2009
Accepted: 21 April 2010
Published: 21 April 2010
Hughes-Stovin syndrome is a very rare disease with fewer than 30 cases reported in the literature. The disease is thought to be a variant of Behcet's disease and is defined by the presence of pulmonary artery aneurysm in association with peripheral venous thrombosis.
A previously healthy 23-year-old Saudi woman presented with massive hemoptysis a day prior to her admission to our hospital. She had a six-month history of recurrent fever, cough, dyspnea, and recurrent oral ulceration. Contrast-enhanced computed tomography scan of her chest and pulmonary angiogram demonstrated a single right-lower lobe pulmonary artery aneurysm. She underwent thoracotomy and right lower lobe resection. Her postoperative course was complicated by deep vein thrombosis. She also developed headache and papilledema, while a magnetic resonance imaging of her brain suggested vasculitis. Based on these clinical presentations, she was diagnosed and treated with Hughes-Stovin syndrome.
The majority of cases of Hughes-Stovin syndrome are reported among men, with only two cases occurring in women. A case of Hughes-Stovin syndrome occurring in a woman is presented in this report. She was treated successfully with multimodality treatment that includes surgery, steroids and cytotoxic agents.
The combination of pulmonary artery aneurysm and thromboembolic disease is uncommon but is reported in association with Behcet's disease [1–5]. The disease affects mainly adults, especially men [1–3]. It is prevalent in Japan, the Middle East, and the Mediterranean but it is also found worldwide [1–4]. Behcet's disease is a form of systemic vasculitis affecting mainly the venules [1–4]. No laboratory tests are diagnostic of Behcet's disease; hence the diagnosis is made based on clinical criteria. The patient must have recurrent oral ulceration with at least two of the following: recurrent genital ulceration, eye lesions, skin lesions, or a positive pathergy test [1, 6].
In 1911, Beattie and Hall reported the association between multiple aneurysms of the pulmonary arteries and venous thrombosis of the lower limbs . The same combination was reported later by Hughes and Stovin in 1959 . They reported four cases of deep venous thrombosis and multiple segmental pulmonary artery aneurysms. Since then, this association has been named Hughes-Stovin syndrome. Hughes-Stovin syndrome occurs very rarely, with fewer than 30 cases reported in the literature [9, 10]. It affects mainly men, with only two cases describing women . Patients usually present with fever, chills, dyspnea, cough, hemoptysis, and venous thrombosis [9, 10].
The main cause of death in Hughes-Stovin syndrome is massive hemoptysis secondary to the rupture of A pulmonary artery aneurysm [9, 10, 12]. The pathogenesis of Hughes-Stovin syndrome is unclear, although many hypotheses have been made to explain the manifestations of this syndrome. It has been suggested that pulmonary artery aneurysms may arise from a degenerative defect in the bronchial arteries or may be mycotic in origin resulting from emboli infected with low-grade virulence organisms. It may also be due to angiodysplasia of the bronchial arteries [9, 11]. However, none of these hypotheses are widely accepted.
It is currently thought that Hughes-Stovin syndrome is a form of vasculitis similar to Behcet's disease [5, 9, 13, 14]. In reality, Behcet's disease and Hughes-Stovin syndrome are the only vasculitides known to cause pulmonary artery aneurysms in patients [1, 3, 12]. Many authors have even suggested that Hughes-Stovin syndrome may represent a variant of Behcet's disease [3, 5, 15].
Because she complained of intermittent headache over the past six months, a CT scan of the brain with contrast was done. It revealed no abnormalities. However, a magnetic resonance imaging (MRI) scan of the brain showed increased high-intensity signals bilaterally especially in the gray/white matter junction (>4 foci) in fluid-attenuated inversion recovery (FLAIR) images. This was highly suggestive of vasculitis.
She then underwent right thoracotomy with the removal of her right lower lobe. Pathological examination revealed multifocal arterial thrombosis with marked luminal narrowing, partial destruction of her arterial wall, and marked intimal fibrosis (fibroelastosis).
Our patient's postoperative course was uneventful. A few days later, however, she developed swelling in her right lower limb. Doppler sonography revealed deep vein thrombosis in her right iliac, right common femoral, right superficial femoral and right popliteal veins. Spiral CT scan of her chest showed a small filling defect in her right apical segmental artery consistent with pulmonary embolism. She was thus commenced on intravenous unfractionated heparin followed by oral coumadin.
An ophthalmologic examination of our patient showed no evidence of iritis or retinal vasculitis. However, she was found to have optic disc swelling (papilledema). She was thus diagnosed with Hughes-Stovin syndrome, which is a variant of Behcet's disease. She was treated with methylprednisolone 1 gm intravenously for five days. She then had 50 mg/day of oral azathioprine. Her dosage increased gradually to 150 mg/day, with 0.5 mg bid of colchicines. A repeat MRI of her brain three weeks after the treatment showed complete resolution of the high intensity signals in FLAIR images, thus indicating her favorable response to treatment. Repeat spiral CT scans of her chest for the succeeding 12 months revealed no recurrence of pulmonary aneurysm.
Hughes-Stovin syndrome is considered a variant of Behcet's disease [3, 5]. Both diseases are characterized by the destruction of the wall of the pulmonary arteries and perivascular infiltration. Nearly 25% of patients with Hughes-Stovin syndrome develop vascular thromboembolism, arterial aneurysms, and arterial and venous occlusions with nonspecific vasculitis. The vascular lesions are arterial in 7%, venous in 25%, and both in 68% of reported cases [1, 4, 16]. Arterial aneurysm is often associated with the poor prognosis of patients, and is usually found present in the pulmonary arteries and in the aorta [1, 4, 12, 16].
Pulmonary involvement is seen in 1% to 7% of reported cases. Pulmonary lesions, which are seen in Behcet's disease, are pulmonary arterial aneurysms, arterial-venous thrombosis, pulmonary infarcts, focal atelectasis, and occasionally pleural effusions. Pulmonary vasculitis is multifocal and thrombosis is seen in the branches of pulmonary arteries [1, 2, 4].
Our patient described in this case report has only a single aneurysm. Aneurysms may be single or multiple, unilateral or bilateral. It is rarely multiple or bilateral. Reports indicate that pulmonary lesions and deep venous thrombosis of the lower extremities are the most frequent findings [5, 17]. The exact mechanism of thrombosis in Behcet's disease is unknown. Thrombophilia does not seem to play a major role in the notable tendency among patients with Behçet's disease to develop thrombosis. However, hyperhomocysteinemia is also assumed to be an independent factor in the development of venous thrombosis [18, 19].
In the patient described in this case report, anticoagulants were used to safely treat her deep vein thrombosis after her pulmonary artery aneurysm was resected (right lower lobectomy). Surgical resection has also been performed in some cases. However, it may be difficult to perform it if there are multiple or bilateral aneurysms . The embolization of pulmonary artery aneurysms has been reported by many authors [5, 9, 11, 17]. The advantages of embolization are that it is less invasive and has the ability to treat multiple and bilateral aneurysms. Corticosteroids, alone or in combination with cytotoxic drugs, have been tried in patients with Hughes-Stovin syndrome [4, 9, 17]. Although found to be effective in some cases, they were not always useful in preventing disease progression particularly in the late stages of the disease .
Our patient described in this case report underwent right lower lobectomy with an uneventful postoperative course. She was treated with pulse steroid in combination with azathioprine. She responded well to treatment and remains in complete remission.
Written informed consent was obtained from our patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
I would like to thank my colleagues, consultant rheumatologist Saleh Moteyee and thoracic surgeon Nizar Yamani, who contributed in the case diagnosis and management. I also would like to thank pulmonary consultant Nehad Shirawi for helping me prepare the text and the figures contained in this manuscript.
- Erkan E, Gul A, Tasali E: Pulmonary manifestations of Behcet's disease. Thorax. 2001, 56: 572-578. 10.1136/thorax.56.7.572.View ArticlePubMedPubMed CentralGoogle Scholar
- Kontogrannis V, RJ P: Behcet's disease. Postgrad Med J. 2000, 76: 629-637. 10.1136/pmj.76.900.629.View ArticleGoogle Scholar
- Bowman S, Honey M: Pulmonary arterial occlusions and aneurysms: a forme fruste of Behcet's or Hughes-Stovin syndrome. British Heart Journal. 1990, 63 (1): 66-68. 10.1136/hrt.63.1.66.View ArticlePubMedPubMed CentralGoogle Scholar
- Efthimou J, Johnston C, Spiro SG, Turner-Warwick M: Pulmonary Disease in Behcet's syndrome. QJ Med. 1986, 58: 259-280.Google Scholar
- Emad Y, Ragab Y, Shawki Ael H, Gheita T, El-Marakbi A, Salama MH: Hughes-Stovin syndrome: is it incomplete Behcet's? Report of two cases and review of the literature. Clin Rheumatol. 2007, 26 (11): 1993-1996. 10.1007/s10067-007-0609-y.View ArticlePubMedGoogle Scholar
- Grana Gil J, Sanchez Meizoso MO: Diagnostic criteria and differential diagnosis of Behcets disease. Revista Clinica Espanola. 2002, 202 (1): 20-22.View ArticlePubMedGoogle Scholar
- Hughes JP, PGI S: Segmental pulmonary artery aneurysms with peripheral venous thrombosis. Br J Dis Chest. 1959, 53: 19-27. 10.1016/S0007-0971(59)80106-6.View ArticlePubMedGoogle Scholar
- Weintraub JL, DeMayo R, Haskal ZJ, J S: SCVIR annual meeting film panel session: diagnosis and discussion of case 1: Hughes-Stovin syndrome. J Vasc Interv Radiol. 2001, 12 (4): 53153-4. 10.1016/S1051-0443(07)61897-1.View ArticleGoogle Scholar
- Ammann ME, Karnel F, Olbert F, Mayer K: Radiologic findings in the diagnosis of Hughes-Stovin syndrome. Ajr. 1991, 157 (6): 1353-4.View ArticlePubMedGoogle Scholar
- Mahlo HR, Elsner K, Rieber A, Brambs HJ: New approach in the diagnosis of and therapy for Hughes-Stovin syndrome. Ajr. 1996, 167 (3): 817-818.View ArticlePubMedGoogle Scholar
- Roberts DH, Jimenez JF, Golladay ES: Multiple pulmonary artery aneurysms and peripheral venous thromboses: the Hughes Stovin syndrome. Report of a case in a 12-year-old boy and a review of the literature. Pediatric Radiol. 1982, 12 (4): 214-216. 10.1007/BF00999315.View ArticleGoogle Scholar
- Yazici HFE: Mortality in Behçet's syndrome. Clin Exp Rheumatol. 2008, 26: S138-S140.PubMedGoogle Scholar
- Erkan D, Yazici Y, Sanders A, Trost D, H Y: Is Hughes-Stovin syndrome Behçet's disease?. Clin Exp Rheumatol. 2004, 22 (4 Suppl 34): S64-S68.PubMedGoogle Scholar
- Francois MF: Is Hughes-Stovin syndrome a particular expression of Behcet's disease?. Chest. 1983, 83 (2): 288-10.1378/chest.83.2.288a.View ArticlePubMedGoogle Scholar
- Erkan D, Yazici Y, Sanders A, Trost D, Yazici H: Is Hughes-Stovin syndrome Behcet's disease?. Clin Exp Rheumatol. 2004, 22 (4 Suppl 34): S64-S68.PubMedGoogle Scholar
- Uzun Oguz, Akpolat Tekin, Erkan Levent: Pulmonary vasculitis in Behcet disease: a cumulative analysi. Chest. 2005, 127: 2243-2253. 10.1378/chest.127.6.2243.View ArticlePubMedGoogle Scholar
- Lee J, Noh JW, Hwang JW, Kim H, Ahnn JK, Koh EM, Cha HS: Successful cyclophosphamide therapy with complete resolution of pulmonary artery aneurysm in Hughes-Stovin syndrome patient. Clin Rheumatol. 2005, 570 (11): 570-Google Scholar
- Aksu K, Turgan N, Oksel F, Keser G, Ozmen D, Kitapcioglu G, Gumusdis G, Bayindir O, Doganavsargil E: Hyperhomocysteinaemia in Behcet's disease. Rheumatology (Oxford). 2000, 40: 687-690. 10.1093/rheumatology/40.6.687.View ArticleGoogle Scholar
- Leiba M, Seligsohn U, Sidi Y, Harats D, Sela BA, Griffin JH, Livneh A, Rosenberg N, Gelernter I, Gur H, Ehrenfeld M: Thrombophilic factors are not the leading cause of thrombosis in Behçet's disease. Ann Rheum Dis. 2004, 63 (11): 1445-1449. 10.1136/ard.2003.014241.View ArticlePubMedPubMed CentralGoogle Scholar
- Tunaci M, Ozkorkmaz B, Tunaci A, Gul AEGBA: CT findings of pulmonary artery aneurysms during treatment for Behcet's disease. The American Journal of Roentgenology, Radium Therapy and Nuclear Medicine. 1999, 172: 729-733.View ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.