Acute neurological signs as the predominant clinical manifestation in four dogs with Angiostrongylus vasorum infections in Denmark
© Gredal et al; licensee BioMed Central Ltd. 2011
Received: 1 June 2010
Accepted: 28 June 2011
Published: 28 June 2011
Four dogs with acute neurological signs caused by haemorrhages in the central nervous system were diagnosed with Angiostrongylus vasorum infection as the underlying aetiology. Two dogs presented with brain lesions, one dog with spinal cord lesions and one with lesions in both the brain and spinal cord. Only one dog presented with concurrent signs of classical pulmonary angiostrongylosis (respiratory distress, cough), and only two dogs displayed overt clinical signs of haemorrhages. Results of coagulation assays were inconsistent. Neurological signs reflected the site of pathology and included seizures, various cranial nerve deficits, vestibular signs, proprioceptive deficits, ataxia and paraplegia. One dog died and three were euthanised due to lack of improvement despite medical treatment. This emphasises canine angiostrongylosis as a potential cause of fatal lesions of the central nervous system and the importance of including A. vasorum as a differential diagnosis in young dogs with acute neurological signs in Denmark.
Angiostrongylus vasorum, also known as the French heartworm, is an approximately 13-21 millimetre gastropod-borne nematode, recognised in endemic areas of Europe [1–8], North and South America [9–12] and Uganda [13, 14]. In endemic areas, the parasite is a well-known cause of respiratory disease (canine pulmonary angiostrongylosis, CPA) especially in young dogs which, along with other canine species, e.g. the fox, act as the definitive hosts in the life cycle of the parasite [1, 3, 15]. The adult worms primarily inhabit the pulmonary arteries and right cardiac ventricle of the canine host, resulting in a verminous pneumonia with obliterative thrombotic endarteritis and fibrosis . The primary clinical signs are reported to be cough, exercise intolerance, dyspnoea and right sided heart failure, all of which are directly related to the respiratory system. However, non-specific clinical signs such as vomiting, diarrhoea or anorexia are also frequently reported . Furthermore, disorders of haemostasis resulting in severe haemorrhages have been identified as possible complications of the CPA complex [3, 15]. The exact pathophysiological mechanisms remain unclear [3, 15], but a chronic low grade disseminated intravascular coagulation (DIC) with associated consumption of both platelets and coagulation factors is most commonly suggested [17, 18]. Immunemediated thrombocytopenia associated with A. vasorum infections has also been reported as a possible cause of bleedings . Prolongation of clotting times and decrease of coagulation factors, e.g. von Willebrand factor and factor V have been reported in both experimentally and naturally infected animals, although not consistently [17, 20, 21].
A minor proportion (approximately 4%) of CPA patients present with neurological signs [3, 15]. Acute neurological signs including ataxia, paresis, paralysis, or seizures seem to result primarily from haemorrhages in the central nervous system (CNS) caused by the parasitic induced haemostatic disorder [2, 22–25]. This has previously been reported from the United Kingdom [20, 22, 23, 26] and Germany . However, migrating larvae, causing focal damage to the nervous tissue have also been reported [25, 27]. A recent case report suggests that A. vasorum may cause an inflammatory response of the CNS resembling that of a meningitis or meningoencephalitis .
Previous investigations of populations of clinically affected CPA patients, including dogs with neurological signs, report a median age of 10 to 18 months [15, 29]. Neurological signs in young dogs often give rise to a suspicion of congenital/hereditary conditions or immune-mediated meningitis/meningo-encephalitis, whereas CPA may easily be overlooked as a differential diagnosis, potentially resulting in a fatal outcome in these young dogs.
Neurological cases of dogs with A. vasorum have not previously been reported from Denmark. The purpose of the present study was therefore to draw attention to A. vasorum infections as a potential cause of acute neurological disease in dogs in Denmark. We describe the diagnostic work-up, medical treatment and outcome in four dogs, presenting with neurological signs caused by CNS haemorrhages associated with haemostatic dysfunction in dogs infected with A. vasorum.
All cases were seen at the small animal hospital, University of Copenhagen, Denmark. A summary of the clinical data and blood results can be appreciated from Additional file 1: Table S1 and Additional file 2: Table S2.
A 31/2-year-old male Welsh Corgi was presented as an emergency with severe ataxia of acute onset a few hours prior to admission. A clinical examination revealed a bleeding wound in the tongue. The dog had previously been investigated for haemostatic dysfunction due to recurring episodes of prolonged bleeding and subcutaneous haemorrhages within six months of the acute neurological event. An underlying cause was not identified at the time and no medical treatment was given.
The dog presented non-ambulatory, mentally depressed and with tonic-clonic seizures. There was spontaneous nystagmus, changing between rotatory and vertical, and all limbs were slightly hypertonic. Postural reactions were not tested as the dog was non-ambulatory. These findings indicated one or more neurological lesions located to the vestibular system (central or peripheral) and/or the cerebellum in addition to cerebrocortical involvement.
Routine biochemistry revealed hypercalcaemia and hyperglycaemia, but other results were within normal references (additional file 2). Regrettably, haematology and coagulation times were not performed at this point in time. Previous laboratory results had revealed normal platelet counts and marginally elevated coagulation times in addition to increased D-dimers (8.7) (additional file 2).
Due to a history of recurrent signs of haemostatic dysfunction, a brain haemorrhage was considered the most likely cause of acute neurological disease, although the underlying bleeding disorder had not been characterised. However, neuroimaging was not available at the hospital for further diagnostic work-up.
The dog was hospitalised for supportive care (intravenous (IV) fluids and oxygen) and anticonvulsant therapy (diazepam at 1 mg/kg IV, phenobarbitone at 3 mg/kg with a subsequent administration 1 h later). Unfortunately, the dog deteriorated continuously and was euthanised on the same day at the owner's request.
Necropsy and histopathology of the brain (haematoxylin and eosin (H&E)) demonstrated the presence of acute disseminated haemorrhages throughout the brain and meninges, with larger solitary bleedings located to the right part of the cerebellum, and to the left caudate nucleus and the internal capsule. Furthermore, acute malacic foci and foci of gitter and glial cells, oedema and proliferation of capillaries/venules were demonstrated throughout the brain, including the cerebral cortex. Moderate cuffing and meningeal infiltrates of macrophages and lymphocytes/plasma cells and neutrophils were also present. Additionally, a larval granuloma was recorded in the encephalon.
In the lungs, multiple adult A. vasorum worms and thrombosis of pulmonary arteries with proliferation of the intima layer were acknowledged. Interstitial pulmonary fibrosis and granulomas with infiltrating macrophages as the predominant cell type and a central content of eggs or larvae were found throughout the lung tissue.
An eleven-months-old male Basset Hound was referred as an emergency with a two-week-history of respiratory signs, including tachypnoe and coughs, and an acute onset of tonic-clonic seizures with reduced consciousness 24 h prior to presentation.
On presentation the dog was mentally depressed and non-ambulatory tetraparetic and showed severe respiratory signs. Neurological signs progressed rapidly and a few hours after presentation the dog was semi-comatous with absence of pupillary light reflexes (PLR) and anisocoria. Given a history of seizures and rapidly progressing mental changes, cerebrocortical pathology causing increased intracranial pressure and possible brain stem affection, was suspected.
Thoracic radiographs displayed signs of focal lung pathology in the caudal lung lobes which could indicate A. vasorum infection. A diagnosis was verified by a faeces smear containing multiple L1 larvae. Routine haematology revealed a reduced packed cell volume (PCV) of 0.33 and a platelet count of 97 × 109/L. Activated partial thromboplastin time (APTT) was normal and prothrombin time (PT) and D-dimer were only slightly elevated (additional file 2). Given the diagnosis of severe pulmonary angiostrongylosis and thrombocytopenia, a CNS haemorrhage was considered likely, although no overt bleedings were present. Intoxication was also considered, but was highly unlikely according to the owner. Intensive supportive medical care and imidacloprid 10%/moxidectin 2.5% (Advocate spot-on) at 0.1 ml/kg were instituted, but the dog deteriorated and died within hours of admission to the hospital.
In the kidneys, a single larval granuloma was identified.
A seven-months-old Danish/Swedish farmdog was referred with progressive ataxia and mucosal membrane petechiae of 24 h duration. A diagnosis of A. vasorum had already been established by a faeces smear performed by the local veterinarian 24 h prior to referral. On presentation, the dog was alert but non-ambulatory paraplegic and in pain. Petechial haemorrhages were present in both scleras, and oral and ocular mucosal membranes. The neurological examination revealed no cranial nerve deficits. Both thoracic limbs were hypertonic and there was a bilateral flaccid paralysis of the pelvic limbs. Proprioceptive placing reactions were normal in the thoracic limbs but absent in the pelvic limbs. Patellar and withdrawal reflexes were bilaterally absent in the pelvic limbs, but the perineal reflex was preserved. Cutaneous trunci reflex was normal. Neurological signs seemed compatible with Schiff-Sherrington syndrome, and a T3-L3 lesion was suspected. However, as the cutaneous trunci lesion was normal in the T3-L3 region, multifocal disease was considered with a possible lesion cranial to C6, giving rise to upper motor neuron signs of the thoracic limbs, and a second lesion in the lumbosacral plexus (L4-S2) causing lower motor neuron signs of the pelvic limbs.
Thoracic radiographs showed a diffuse interstitial lung pattern. Haematology revealed a decrease in PCV (0.34), thrombocytopenia (103 × 109/L), and increased D-dimers (2.0). Prothrombin time was prolonged (9.1) but APTT was only mildly increased (10.9) (additional file 2). The clinical findings of scleral and mucosal membrane haemorrhages strongly suggested the neurological signs to be caused by acute CNS haemorrhages. Based on previous experiences, A. vasorum was considered a likely cause of haemostatic dysfunction although other disorders such as von Willebrand deficiency and acute warfarin poisoning were also considered. The dog showed no improvement despite intensive treatment with IV fluids, plasma transfusion, fenbendazole (at 20 mg/kg once a day (SID)), methadone and prednisolone acetate IV (at 1 mg/kg SID). It was therefore euthanised at the owners' request after two days of hospitalisation.
A 10-month-old Labrador-Cross, female, was referred for investigation of rapidly progressing pelvic limb paresis and lumbosacral pain of four days duration.
Surgical spinal cord decompression at L4-L6 was considered, but did not seem a reasonable option given the risk of severe haemorrhages. The dog was therefore treated medically with plasma transfusions, fenbendazole at 20 mg/kg SID, prednisolone at 1 mg/kg SID for 3 days, methadone and physiotherapy for 6 days. However, as no improvement of the neurological status was recognised, the dog was euthanised at the owner's request.
At necropsy, an acute intramedullary haemorrhage was identified at the level of the caudal lumbar segments. In addition, several microscopic haemorrhages in the spinal cord were identified by histopathology (H&E). Occasionally, acute malacic foci were seen, as well as foci of gitter and glial cells, and proliferation of capillaries/venules. Moderate cuffing (macrophages, lymphocytes/plasma cells and neutrophils) and dense focal infiltrates of neutrophils (absence of eosinophilic granules by Luna staining) were furthermore encountered. Histopathological findings of the lungs were comparable to those of the previous cases. In the kidney a larva without any inflammatory reaction was seen within a small size vessel.
CPA is a commonly diagnosed disease in endemic areas of Denmark and the UK, primarily presenting as respiratory disease [3, 15]. The included cases of the present study all presented with neurological signs as the primary complaint, in each patient caused by one or more CNS haemorrhages resulting from haemostatic dysfunction associated with A. vasorum and/or evidence of aberrant larvae. This emphasises CPA as an important differential diagnosis in dogs presenting with neurological signs of unknown aetiology. Acute non-traumatic brain haemorrhages are only infrequently reported in dogs , and A. vasorum should therefore be highly suspected as the underlying cause of brain haemorrhages in endemic areas. As opposed to ischaemic stroke, which appear with greater frequency and which might present with similar neurological signs, CPA is most commonly seen in young dogs [3, 15], whereas the mean age of dogs reported with ischaemic stroke is 8.4-8.9 years [31, 32]. The mean age of dogs in the present study was 10 months (median; 17 months) which is in accordance with previous studies of dogs naturally infected with A. vasorum[3, 15]. The present study furthermore confirms haemorrhages due to A. vasorum to be an important differential diagnosis to acute disc disease and fibrocartilaginous embolisation in dogs with acute spinal cord disease in endemic areas as previously reported [23, 33].
On clinical examination, only one dog (case 2) exhibited respiratory signs as part of the clinical pattern, and only two dogs (cases 1 and 3) had visible signs of an ongoing bleeding disorder. One of these dogs (case 1) had primarily haematomas, a characteristic clinical sign observed in connection with coagulopathies, whereas one dog (case 3) presented with mucosal petecchiation, a sign most often associated with disorders of primary haemostasis such as thrombocytopenia. Thus, CPA may easily be missed as the underlying aetiology due to the lack of classic respiratory signs or overt clinical signs of haemorrhages in dogs with acute neurological disease.
As opposed to dogs mildly to moderately infected (i.e. with no signs of coagulopathy or neurological disease), in which survival is close to 100% [3, 15], the prognosis of CPA should be considered guarded when complicated by haemostatic dysfunction and even more so when the condition gives rise to severe neurological deficits. This can also be appreciated from a review of neurological cases in which 11 out of 17 (65%) died despite recognition and treatment of A. vasorum in the majority [2, 20, 22, 23, 25, 26, 28, 33, 34]. Compromised blood supply to the area involved, along with direct physical compression caused by a haematoma makes the CNS, which is strongly dependent on continuous supplies of oxygen and glucose, highly susceptible to irreversible damage. Furthermore, any attempt of surgical decompression or evacuation of the haematoma is severely complicated by the presence of ongoing haemostatic dysfunction unless addressed appropriately by blood component therapy such as fresh frozen plasma or cryoprecipitate .
In the present report all patients suffered from haemostatic dysfunction related to the parasitic infection according to the laboratory analysis, and all had a fatal outcome. Case 1 was seen back in 2000 when CPA was largely unknown in Denmark. Retrospectively viewed, CPA should have been considered the underlying aetiology of the coagulopathy when the dog first presented with subcutaneous haemorrhages only. Chances of a successful treatment at this early stage had probably been favourable.
In case 2 the dog deteriorated rapidly upon admittance despite appropriate diagnostic work-up and treatment. With thrombocytopenia, a low fibrinogen, a prolonged APTT and increased D-dimers the dog appeared to suffer a state of irreversible DIC resulting in a severe consumptive coagulopathy which was refractory to medical treatment, stressing the severe complications of A. vasorum infections . Also notable in this case were the chronic histopathological changes indicating that the cerebral haematoma had been present for 7-10 days although acute neurological signs were not noticed until the day prior to submission. This emphasises the importance of early recognition and treatment of A. vasorum in dogs displaying other signs of CPA e.g. respiratory disease as in the present case.
In cases 3 and 4 the neurological condition caused by CPA did not appear to be fatal, but the dogs were euthanised as the prognosis with regard to full recovery and ambulation was guarded in both. Thus, death may not result directly from the haemorrhage itself, but euthanasia may be reasoned by the severe and irreversible disabilities caused by the haemorrhage.
On haematology, cases 2-4 presented with anaemia and thrombocytopenia. These results differ from findings in most mildly to moderately affected CPA patients [15, 37] but have been reported in several neurological patients with haemostatic dysfunction [2, 22] and in the study of experimentally infected dogs by Cury and others . Regrettably, haematology and coagulation times were not performed at the final consult of case 1.
Eosinophilic counts were within normal ranges for all cases as opposed to the findings by Cury and others  and Chapman and others . Although an eosinophilic response is to be expected with parasitic diseases , some studies report eosinophilia as a less frequent finding in A. vasorum cases. In this respect, Willesen and others found that only 21% of the dogs had eosinophilia at the time of diagnosis . In addition, histopathology of the present cases demonstrated the absence of eosinophilia which is in accordance with previous reports of absent or only mild eosinophilia [2, 27]. The exact mechanisms for this lack of eosinophilic response remain unclear, but have been suggested to be associated with either low grade infections or more chronic states [39, 40].
D-dimers were analysed in cases 2-4 when they presented as neurological emergencies, and had previously been tested in case 1, and found elevated in all cases. A normal D-dimer level is known to be a valuable marker when ruling out deep venous thrombosis, pulmonary thromboembolism and DIC [36, 41]. The findings of elevated D-dimers imply that DIC cannot be excluded as part of the underlying mechanism of A. vasorum induced coagulopathies.
Biochemistry revealed elevated levels of bilirubin in three cases, but otherwise normal results. Hyperbilirubinaemia, in the absence of elevated liver enzymes, is possibly the result of increased haemolysis in these suspected DIC patients. Previous reports of decreased levels of serum fructosamine and increased levels of serum globulin in CPA were generally not confirmed in this study [15, 37, 42]. Hyperglobulinaemia was only present in one case (case 4) (25%) as opposed to the findings by Chapman and others in which 70% had elevated serum globulins . Hypercalcaemia was found in cases 1 and 3. This finding has previously been reported in association with Angiostrongylus infections in dogs and has been suggested to be the result of granulomatous disease . As all dogs in the present study died, changes in calcium levels with antiparasitic treatment could not be followed.
This report of four dogs infected with A. vasorum documents the importance of A. vasorum infection as a differential diagnosis, particularly in young dogs with acute neurological signs of unknown aetiology in Denmark. The identification of A. vasorum as the underlying cause of a primary presentation of neurological disease is complicated by the fact that dogs may display neither visible clinical signs of haemostatic dysfunction nor the classical respiratory signs of CPA.
We suggest that a Baermann test is performed in any dog with unexplainable neurological signs in endemic areas. Due to the intermittent shedding of A. vasorum larvae we advice testing of faeces samples from three consecutive days in order to increase the sensitivity of the test.
Written informed consent was obtained from the owners for publication of this case report.
Ulrik Westrup (DVM, ECVDI Resident, University of Copenhagen) is kindly acknowledged for MRI evaluations in case 4.
- Bolt G, Monrad J, Koch J, Jensen AL: Canine angiostrongylosis: a review. Vet Rec. 1994, 135: 447-452. 10.1136/vr.135.19.447.View ArticlePubMedGoogle Scholar
- Denk D, Matiasek K, Just FT, Hermanns W, Baiker K, Herbach N, Steinberg T: Disseminated angiostrongylosis with fatal cerebral haemorrhages in two dogs in Germany: A clinical case study. Vet Parasitol. 2009, 160: 100-108. 10.1016/j.vetpar.2008.10.077.View ArticlePubMedGoogle Scholar
- Koch J, Willesen JL: Canine pulmonary angiostrongylosis: An update. Vet J. 2009, 179: 348-359. 10.1016/j.tvjl.2007.11.014.View ArticlePubMedGoogle Scholar
- Martin MWS, Neal C: Distribution of angiostrongylosis in Cornwall. J Small Anim Pract. 1992, 33: 327-330. 10.1111/j.1748-5827.1992.tb01158.x.View ArticleGoogle Scholar
- Papazahariadou A, Founta A, Papadopoulos E, Chliounakis S, Antoniadou-Sotiriadou K, Theodorides Y: Gastrointestinal parasites of shepherd and hunting dogs in the Serres Prefecture, Northern Greece. Vet Parasitol. 2007, 148: 170-173. 10.1016/j.vetpar.2007.05.013.View ArticlePubMedGoogle Scholar
- Roche MM, Kelliher DJ: Angiostrongylus vasorum infestation in a dog: A case report. Irish Vet J. 1968, 22: 108-113.Google Scholar
- Segovia JM, Torres J, Miquel J, Llaneza L, Feliu C: Helminths in the wolf, Canis lupus, from north-western Spain. J Helminthol. 2001, 75: 183-192.PubMedGoogle Scholar
- Trees AJ: Angiostrongylus vasorum in dogs in Wales. Vet Rec. 1987, 120: 424-Google Scholar
- Conboy G: Natural infections of Crenosoma vulpis and Angiostrongylus vasorum in dogs in Atlantic Canada and their treatment with milbemycin oxime. Vet Rec. 2004, 155: 16-18. 10.1136/vr.155.1.16.View ArticlePubMedGoogle Scholar
- Jeffery RA, Lankester MW, McGrath MJ, Whitney HG: Angiostrongylus vasorum and Crenosoma vulpis in red foxes (Vulpes vulpes) in Newfoundland, Canada. Can J Zool. 2004, 82: 66-74. 10.1139/z03-211.View ArticleGoogle Scholar
- Lima WS, Guimaraes MP, Lemos IS: Occurrence of Angiostrongylus vasorum in the lungs of the Brazilian fox Dusicyon vetulus. J Helminthol. 1994, 68: 87-10.1017/S0022149X00013547.View ArticlePubMedGoogle Scholar
- Oliveira SD, Barcante JMP, Barcante TA, Ribeiro VM, Lima WS: Ectopic location of adult worms and first-stage larvae of Angiostrongylus vasorum in an infected dog. Vet Parasitol. 2004, 121: 293-296. 10.1016/j.vetpar.2004.02.018.View ArticleGoogle Scholar
- Bwangamo O: Angiostrongylus vasorum and other worms in dogs in Uganda. Vet Rec. 1972, 91: 267-268. 10.1136/vr.91.11.267.View ArticleGoogle Scholar
- Bwangamo O: Renal, lymphoid and pulmonary lesions in naturally acquired canine angiostrongylosis in Uganda. Bull Epizoot Dis Afr. 1974, 22: 55-68.Google Scholar
- Chapman PS, Boag AK, Guitian J, Boswood A: Angiostrongylus vasorum infection in 23 dogs (1999-2002). J Small Anim Pract. 2004, 45: 435-440. 10.1111/j.1748-5827.2004.tb00261.x.View ArticlePubMedGoogle Scholar
- Prestwood AK, Greene CE, Mahaffey EA, Burgess DE: Experimental canine angiostrongylosis: I. Pathologic manifestations. J Am Anim Hosp Assoc. 1981, 17: 491-497.Google Scholar
- Cury MC, Lima WS, Guimaraes MP, Carvalho MG: Hematological and coagulation profiles in dogs experimentally infected with Angiostrongylus vasorum (Baillet, 1866). Vet Parasitol. 2002, 104: 139-149. 10.1016/S0304-4017(01)00616-1.View ArticlePubMedGoogle Scholar
- Ramsey IK, Littlewood JD, Dunn JK, Herrtage ME: Role of chronic disseminated intravascular coagulation in a case of canine angiostrongylosis. Vet Rec. 1996, 138: 360-363. 10.1136/vr.138.15.360.View ArticlePubMedGoogle Scholar
- Gould SM, McInnes EL: Immune-mediated thrombocytopenia associated with Angiostrongylus vasorum infection in a dog. J Small Anim Pract. 1999, 40: 227-232. 10.1111/j.1748-5827.1999.tb03068.x.View ArticlePubMedGoogle Scholar
- Whitley NT, Corzo-Menendez N, Carmichael NG, McGarry JW: Cerebral and conjunctival haemorrhages associated with von Willebrand factor deficiency and canine angiostrongylosis. J Small Anim Pract. 2005, 46: 75-78. 10.1111/j.1748-5827.2005.tb00296.x.View ArticlePubMedGoogle Scholar
- Schelling CG, Greene CE, Prestwood AK, Tsang VCW: Coagulation abnormalities associated with acute Angiostrongylus vasorum infection in dogs. Am J Vet Res. 1986, 47: 2669-2673.PubMedGoogle Scholar
- Garosi LS, Platt SR, McConnell JF, Wray JD, Smith KC: Intracranial haemorrhage associated with Angiostrongylus vasorum infection in three dogs. J Small Anim Pract. 2005, 46: 93-99. 10.1111/j.1748-5827.2005.tb00300.x.View ArticlePubMedGoogle Scholar
- Wessmann A, Lu D, Lamb CR, Smyth B, Mantis P, Chandler K, Boag A, Cherubini GB, Capello R: Brain and spinal cord haemorrhages associated with Angiostrongylus vasorum infection in four dogs. Vet Rec. 2006, 158: 858-863. 10.1136/vr.158.25.858.View ArticlePubMedGoogle Scholar
- Whitley NT, Corzo-Menendez N, Carmichael NG, McGarry JW: Cerebral and conjunctival haemorrhages associated with von Willebrand factor deficiency and canine angiostrongylosis. J Small Anim Pract. 2005, 46: 190-View ArticleGoogle Scholar
- Perry AW, Hertling R, Kennedy MJ: Angiostrongylosis with disseminated larval infection associated with signs of ocular and nervous disease in an imported dog. Can Vet J. 1991, 32: 430-431.PubMed CentralPubMedGoogle Scholar
- Yamakawa Y, McGarry JW, Denk D, Dukes-McEwan J, Macdonald N, Mas A, McConnell F, Tatton B, Valentine EG, Wayne J, Williams JM, Hetzel U: Emerging canine angiostrongylosis in northern England: five fatal cases. Vet Rec. 2009, 164: 149-152. 10.1136/vr.164.5.149.View ArticlePubMedGoogle Scholar
- Lepri E, Veronesi F, Traversa D, Conti MB, Marchesi MC, Miglio A, Mandara MT: Disseminated angiostrongylosis with massive cardiac and cerebral involvement in a dog from Italy. Parasitol Res.Google Scholar
- Negrin A, Cherubini GB, Steeves E: Angiostrongylus vasorum causing meningitis and detection of parasite larvae in the cerebrospinal fluid of a pug dog. J Small Anim Pract. 2008, 49: 468-471. 10.1111/j.1748-5827.2008.00570.x.View ArticlePubMedGoogle Scholar
- Willesen JL, Kristensen AT, Jensen AL, Heine J, Koch J: Efficacy and safety of imidacloprid/moxidectin spot-on solution and fenbendazole in the treatment of dogs naturally infected with Angiostrongylus vasorum (Baillet, 1866). Vet Parasitol. 2007, 147: 258-264. 10.1016/j.vetpar.2007.05.001.View ArticlePubMedGoogle Scholar
- Wessmann A, Chandler K, Garosi L: Ischaemic and haemorrhagic stroke in the dog. Vet J. 2009, 180: 290-303. 10.1016/j.tvjl.2007.12.023.View ArticlePubMedGoogle Scholar
- Garosi L, McConnell JF, Platt SR, Barone G, Baron JC, de Lahunta A, Schatzberg SJ: Clinical and topographic magnetic resonance characteristics of suspected brain infarction in 40 dogs. J Vet Intern Med. 2006, 20: 311-321. 10.1111/j.1939-1676.2006.tb02862.x.View ArticlePubMedGoogle Scholar
- McConnell JF, Garosi L, Platt SR: Magnetic resonance imaging findings of presumed cerebellar cerebrovascular accident in twelve dogs. Vet Radio Ultrasound. 2005, 46: 1-10. 10.1111/j.1740-8261.2005.00001.x.View ArticleGoogle Scholar
- Patteson MW, Gibbs C, Wotton PR, Day MJ: Angiostrongylus vasorum infection in seven dogs. Vet Rec. 1993, 133: 565-570.PubMedGoogle Scholar
- Martin MWS, Ashton G, Simpson VR, Neal C: Angiostrongylosis in Cornwall: Clinical presentations of eight cases. J Small Anim Pract. 1993, 34: 20-25. 10.1111/j.1748-5827.1993.tb02570.x.View ArticleGoogle Scholar
- Green D: Management of bleeding complications of hematologic malignancies. Semin Thromb Hemost. 2007, 33: 427-434. 10.1055/s-2007-976178.View ArticlePubMedGoogle Scholar
- Wiinberg B, Jensen AL, Johansen PI, Kjelgaard-Hansen M, Rozanski E, Tranholm M, Kristensen AT: Development of a model based scoring system for canine disseminated intravascular coagulation with independent assessment of sensitivity and specificity. Vet J. 2010, 185: 292-298. 10.1016/j.tvjl.2009.06.003.View ArticlePubMedGoogle Scholar
- Willesen JL, Jensen AL, Kristensen AT, Koch J: Haematological and biochemical changes in dogs naturally infected with Angiostrongylus vasorum before and after treatment. Vet J. 2009, 180: 106-111. 10.1016/j.tvjl.2007.10.018.View ArticlePubMedGoogle Scholar
- Klion AD, Nutman TB: The role of eosinophils in host defense against helminth parasites. J Allergy Clin Immunol. 2004, 113: 30-37. 10.1016/j.jaci.2003.10.050.View ArticlePubMedGoogle Scholar
- Bourque A, Whitney H, Conboy G: Angiostrongylus vasorum infection in a coyote (Canis latrans) from Newfoundland and Labrador, Canada. J Wildl Dis. 2005, 41: 816-819.View ArticlePubMedGoogle Scholar
- Bourque AC, Conboy G, Miller LM, Whitney H: Pathological findings in dogs naturally infected with Angiostrongylus vasorum in Newfoundland and Labrador, Canada. J Vet Diagn Invest. 2008, 20: 11-20. 10.1177/104063870802000103.View ArticlePubMedGoogle Scholar
- Nelson OL: Use of the D-dimer assay for diagnosing thromboembolic disease in the dog. J Am Anim Hosp Assoc. 2005, 41: 145-149.View ArticlePubMedGoogle Scholar
- Willesen JL, Jensen AL, Kristensen AT, Kjelgaard-Hansen M, Jessen R, Koch J: Serum fructosamine concentrations in 59 dogs naturally infected with Angiostrongylus vasorum. J Vet Med A. 2006, 53: 266-269.View ArticleGoogle Scholar
- Boag AK, Murphy KF, Connolly DJ: Hypercalcaemia associated with Angiostrongylus vasorum in three dogs. J Small Anim Pract. 2005, 46: 79-84. 10.1111/j.1748-5827.2005.tb00297.x.View ArticlePubMedGoogle Scholar
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