ABSTRACT
Background: Canine Eosinophilic Pulmonary Granulomatosis (EPG) is a severe form of eosinophilic pulmonary disease that carries a guarded prognosis, responds poorly to therapy and recurs frequently. Most studies have reported a caudal lobar pulmonary distribution and a poorer prognosis in idiopathic cases. Case Description: A 7-year-old dog was presented for persistent cough, hyporexia, and weight loss. Eosinophilia and basophilia were transiently present, and an antigen test for heartworm disease was negative. Radiographic studies, followed by a computed tomography (CT) scan revealed nodular lesions and a large mass in the left cranial lobar region suggestive of neoplasia. Cytological and histopathological evaluation was consistent with EPG. The dog responded positively to corticosteroids and has since remained free of disease. Conclusion: EPG in dogs can resemble primary pulmonary neoplasia with secondary intra-pulmonary metastasis. Contrary to previous reports, idiopathic EPG can present with a cranial pulmonary distribution and respond positively to therapy.
Subject(s)
Carcinoma , Dog Diseases , Dogs , Animals , Hong Kong , Neoplasm Recurrence, Local/veterinary , Lung/pathology , Tomography, X-Ray Computed/veterinary , Carcinoma/veterinary , Dog Diseases/diagnosis , Dog Diseases/drug therapy , Dog Diseases/pathologyABSTRACT
Spondyloarthropathies are a group of chronic inflammatory disorders that involve the joints of the axial skeleton, peripheral joints and have extra-articular manifestations. Treatment includes inhibitors of tumor necrosis factor α. Currently there are five approved inhibitors: a soluble receptor, Etanercept and four monoclonal. Etanercept has very low toxicity with pulmonary adverse reactions being very rare. We present the case of a patient who developed respiratory symptoms and pulmonary infiltrates of rapid evolution after the third dose of treatment with Etanercept.
ABSTRACT
Schistosoma is a parasitic infection that affects many people worldwide. However, pulmonary Schistosomiasis is very rare entity which defined as pulmonary involvement develops in persons living or travelling in endemic areas. We report a rare case of 23-year-old Yamani patient admitted as an emergency with a 1-week history of productive cough, hemoptysis, and chest pain. Chest X-ray and computed tomography scan showed right upper lobe peripheral abscess cavity. All routine blood investigations and interventions such as bronchoscopy and bronchoalveolar lavage failed to confirm the diagnosis. However, he underwent right thoracoscopy and excision of this abscess, which unexpectedly showed in the histopathology of the resected specimen Schistosoma parasite infection.
ABSTRACT
INTRODUCTION: Pulmonary intravascular talcosis is a rare condition occurring in intravenous drug users injecting oral medications. Talc results in a foreign-body granulomatous reaction giving a radiological haematogenic miliary appearance mimicking miliary tuberculosis. Drug users represent a population at risk for both these conditions and their distinction may be challenging. CASE REPORT: We reported the case of a man, 33 year-old, intravenous drug addict, detected by the health services because he was the partner of a person who died of contagious and multi-resistant tuberculosis. Chest X-ray and CT scan showed a typical miliary appearance. Despite negative microbiology, clinical diagnosis of miliary tuberculosis was retained. Due to the lack of radiological improvement despite appropriate antibiotic treatment, re-evaluation and trans-bronchial biopsy were undertaken. The presence of granulomas centered by birefringent foreign bodies in polarized light led to a diagnosis of pulmonary intravascular talcosis. CONCLUSION: In the presence of pulmonary miliary in an intravenous drug addict, intravascular talcosis should be suspected.
Subject(s)
Granuloma, Foreign-Body/etiology , Talc/adverse effects , Vascular Diseases/etiology , Adult , Granuloma, Foreign-Body/diagnosis , Humans , Lung/blood supply , Lung/diagnostic imaging , Lung/pathology , Male , Radiography, Thoracic , Tomography, X-Ray Computed , Vascular Diseases/diagnosisABSTRACT
Inhalation of cosmetic talc can lead to pulmonary foreign-body granulomatosis, though fewer than 10 cases of inhaled cosmetic talc-related pulmonary granulomatosis have been reported in adults. We report the case of a 64-year-old man with diffuse, bilateral pulmonary nodules and ground glass opacities associated with chronic inhalation of cosmetic talc. Transbronchial biopsy showed peribronchiolar foreign-body granulomas. After cessation of talc exposure, the patient demonstrated clinical and radiographic improvement without the use of corticosteroids. This case demonstrates that a conservative approach with cessation of exposure alone, without the use of corticosteroids, can be an effective therapy in cosmetic talc-related pulmonary granulomatosis.
