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1.
Yeungnam University Journal of Medicine ; : 279-284, 2017.
Artigo em Coreano | WPRIM | ID: wpr-222846

RESUMO

Pulmonary artery sarcoma (PAS) is a rare and fatal disease that often mimics chronic thromboembolic pulmonary hypertension (CTEPH); therefore, diagnosis of PAS is often delayed. Herein, a healthy 74-year-old man was presented with a 4-month history of dyspnea. Chest computed tomography showed wall thickening and stenosis in the main pulmonary artery as well as in both proximal pulmonary arteries. In order to differentiate between unusual CTEPH, vasculitis, and PAS, we performed right heart catheterization and pulmonary angiography. The mean pulmonary arterial pressure was 21 mmHg, and there was severe pulmonary artery stenosis. Thrombi on the pulmonary arterial wall lesions were observed in intravascular ultrasound and optical coherence tomography. Furthermore, the patient had a history of deep vein thrombosis. Therefore, we diagnosed unusual CTEPH. After 6 months of rivaroxaban anticoagulation therapy, a chest X-ray revealed a left lower lobe lung mass, and a positron emission tomography later showed hypermetabolic lesions in the main pulmonary artery wall, in both pulmonary arteries walls, in the lung parenchyma, and in the bones. A biopsy of the right proximal humerus lesion revealed undifferentiated intimal sarcoma. Pulmonary sarcoma is rare, but should be considered when differentially diagnosing main pulmonary artery wall thickening and stenosis. A positron emission tomography may aid in this diagnosis.


Assuntos
Idoso , Humanos , Angiografia , Pressão Arterial , Biópsia , Cateterismo Cardíaco , Cateteres Cardíacos , Constrição Patológica , Diagnóstico , Dispneia , Fluordesoxiglucose F18 , Úmero , Hipertensão Pulmonar , Pulmão , Tomografia por Emissão de Pósitrons , Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada , Artéria Pulmonar , Rivaroxabana , Sarcoma , Tórax , Tomografia de Coerência Óptica , Ultrassonografia , Vasculite , Trombose Venosa
2.
Journal of Rheumatic Diseases ; : 43-47, 2017.
Artigo em Inglês | WPRIM | ID: wpr-160551

RESUMO

Pleural effusion is a common pulmonary manifestation of systemic lupus erythematosus (SLE) and often occurs as bilateral exudative pleural effusion. The condition usually responds quickly to corticosteroid therapy. However, massive pleural effusion refractory to immunosuppressive drugs has rarely been reported; thus, the proper therapeutic modality is largely decided on a case-by-case basis. In this case, we describe successful treatment with surgical pleurectomy for massive refractory pleural effusion in a patient with SLE.


Assuntos
Humanos , Lúpus Eritematoso Sistêmico , Derrame Pleural
3.
Yeungnam University Journal of Medicine ; : 279-284, 2017.
Artigo em Coreano | WPRIM | ID: wpr-787060

RESUMO

Pulmonary artery sarcoma (PAS) is a rare and fatal disease that often mimics chronic thromboembolic pulmonary hypertension (CTEPH); therefore, diagnosis of PAS is often delayed. Herein, a healthy 74-year-old man was presented with a 4-month history of dyspnea. Chest computed tomography showed wall thickening and stenosis in the main pulmonary artery as well as in both proximal pulmonary arteries. In order to differentiate between unusual CTEPH, vasculitis, and PAS, we performed right heart catheterization and pulmonary angiography. The mean pulmonary arterial pressure was 21 mmHg, and there was severe pulmonary artery stenosis. Thrombi on the pulmonary arterial wall lesions were observed in intravascular ultrasound and optical coherence tomography. Furthermore, the patient had a history of deep vein thrombosis. Therefore, we diagnosed unusual CTEPH. After 6 months of rivaroxaban anticoagulation therapy, a chest X-ray revealed a left lower lobe lung mass, and a positron emission tomography later showed hypermetabolic lesions in the main pulmonary artery wall, in both pulmonary arteries walls, in the lung parenchyma, and in the bones. A biopsy of the right proximal humerus lesion revealed undifferentiated intimal sarcoma. Pulmonary sarcoma is rare, but should be considered when differentially diagnosing main pulmonary artery wall thickening and stenosis. A positron emission tomography may aid in this diagnosis.


Assuntos
Idoso , Humanos , Angiografia , Pressão Arterial , Biópsia , Cateterismo Cardíaco , Cateteres Cardíacos , Constrição Patológica , Diagnóstico , Dispneia , Fluordesoxiglucose F18 , Úmero , Hipertensão Pulmonar , Pulmão , Tomografia por Emissão de Pósitrons , Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada , Artéria Pulmonar , Rivaroxabana , Sarcoma , Tórax , Tomografia de Coerência Óptica , Ultrassonografia , Vasculite , Trombose Venosa
4.
Korean Journal of Medicine ; : 211-215, 2016.
Artigo em Coreano | WPRIM | ID: wpr-101513

RESUMO

Gastric hepatoid adenocarcinoma is a rare adenocarcinoma that develops in the stomach. The prognosis of gastric hepatoid adenocarcinoma is poorer than that of ordinary gastric adenocarcinoma. Here, we report the first case of human epidermal growth factor receptor 2 (HER2)-positive gastric hepatoid adenocarcinoma in Korea. A 57-year-old male presented with abdominal distension and underwent endoscopic gastric biopsy and percutaneous core needle liver biopsy. The pathological findings were consistent with HER2-positive gastric hepatoid adenocarcinoma. He received six cycles of chemotherapy with cisplatin-capecitabine plus trastuzumab, which is a HER2 targeted agent. After chemotherapy, a follow-up abdominal computed tomography scan showed a partial tumor response. This case emphasizes the importance of using trastuzumab in a patient with HER2-positive gastric hepatoid adenocarcinoma.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Adenocarcinoma , Biópsia , Tratamento Farmacológico , Seguimentos , Coreia (Geográfico) , Fígado , Agulhas , Prognóstico , Receptores ErbB , Estômago
5.
Korean Journal of Medicine ; : 330-333, 2016.
Artigo em Coreano | WPRIM | ID: wpr-8159

RESUMO

There have been a few reports of pneumococcal meningitis complicated by spinal epidural abscess. A 58-year-old female with Streptococcus pneumoniae meningitis underwent a recurrent pleocytosis without apparent clinical deterioration after appropriate antibiotic treatment. Subsequently, she developed a spinal epidural abscess. Spinal epidural abscess is a rare complication of pneumococcal meningitis, and subclinical deterioration of neutrophil-dominant pleocytosis may precede development of a spinal epidural abscess in individuals with bacterial meningitis.


Assuntos
Feminino , Humanos , Pessoa de Meia-Idade , Abscesso Epidural , Leucocitose , Meningites Bacterianas , Meningite Pneumocócica
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