• 검색 결과가 없습니다.

A case of myocarditis associated with Toxocara Canis

N/A
N/A
Protected

Academic year: 2022

Share "A case of myocarditis associated with Toxocara Canis "

Copied!
1
0
0

로드 중.... (전체 텍스트 보기)

전체 글

(1)

308

S-537

A case of myocarditis associated with Toxocara Canis

Department of Internal Medicine, College of Medicine, Dong-A University, Busan, Korea

*

Eun-Bin Kim, Young-Hee Nam, Soo-Keol Lee, Dong-Sub Jeon, Hye-Won Lee

Toxocara canins (T.canis), a common dog roundworms, is one of the causative agents of visceral larva migrans. The clinical manifestations in toxocariasis varies widely from asymptomatic to severe organ injury. Human can be infected by ingestion of encapsulated larvae of T. canis in the tissues of a paratenic host. A few cases of myocarditis associated with T.canis have been reported. We report a rare case of myocarditis associated with eosinopilia caused by T. canis. A 45-year-old female was admitted due to chest pain, recurrent loss of consciousness and general fatigue. Echocardiography showed small amount of pericardial effusion and myocardial wall thickening, and left ventricular ejection fraction was normal. On admission, laboratory finding was normal. However, blood eosinophil count was elevated (3,178/µL) on admission day 2, and which increased up to 3,178/µL on day 7. Systemic corticosteroid was administrated. The antibody titer against T.canis was detected in her serum by enzyme-linked immunosorbent assay, and she had a history of ingestion of raw cow’s stomach 2 month ago. Finally we diagnosed myocarditis caused by T.canis. She was treated with a combination therapy of albendazole and prednisolone. Three days later, the eosinophil count and pericardial effusion decreased, and the patient made a full recovery.

Key words: eosinophilia, toxocara canis, myocarditis

S-538

Two cases of right middle lobe syndrome due to eosinophilic mucus in adults

1Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Internal Medicine,

2Department of radiology, 3pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang, Korea

*

Ha Won Hwang

1

, Joo-Hee Kim

1

, Sunghoon Park

1

, Yong Il Hwang

1

, Seung Hun Jang

1

, Ki-Suck Jung

1

, In Jae Lee

2

, Dong Hoon Kim

3

Right middle lobe syndrome (RMLS) is defined as a recurrent or chronic collapse of the middle lobe of the right lung by certain pathologic conditions. RMLS is a relatively uncommon condition having multiple etiologies and various clinical presentations. Here, we report two cases of RMLS due to the eosinophilic mucus. The first case was a 57-year old female visited our clinic because of non productive cough for 3 weeks developing after upper respiratory tract infection. A chest X-ray showed a persistent consolidation in the right middle lobe despite of treatment with antibiotics over two weeks. The second case was a 52-year old female transferred to our clinic for the treatment of pneumonia. Her respiratory symptoms and radiologic abnormalities were gradually resolved after the administration of antibiotics but still remained RML infiltration on the x-ray. In both cases, chest CT scans showed RML obstruction and bronchoscopic findings were the RML bronchus obstruction by thick and yellowish materials. Pathologic findings showed mucus with many eosinophils and Charcot-Leyden crystals. They had no history of bronchial asthma. Pulmonary function tests were normal as well as negative bronchodilator responses. They showed negative responses to fungal allergens such as Alternaria, Aspergillus, Cladosporium, and Penicillium in both skin tests and specific IgE antibodies using ImmunoCAP.

However, they had eosinophilia in blood and bronchoalveolar larvage fluid and elevated total IgE levels. Once the mucus plugs removed, their symptoms and x-ray were normalized. In conclusion, eosinophilic mucus should be considered as one of the causes in patients with RMLS regardless of typical asthmatic symptoms.

참조

관련 문서

Here, we report a case of acute acalculous cholecystitis with gallbladder perforation after non-typhoidal group D Salmonella infection.. A 71-year-old man was admitted

This is a case report of a 57-year-old woman with spontaneous rupture of renal pelvis without identifiable cause, which was managed successfully by insertion

The authors experienced a case of a huge radicular cyst with maxillary sinus evolution, which was treated with complete resection of the cyst and immediate reconstruction

We report a rare but typical case of GA intoxication associated with anterograde amnesia and bilateral hippocampal involvement.. A 53-year-old woman with GA intoxication presented

Glycogenic hepatopathy (GH) is a rare complication of type 1 diabetes mellitus. We report the case of a 13-year-old diabetic female with poorly controlled blood sugar

Herein, we report a case of prostatic malacoplakia in a 72-year-old man, which was diagnosed on a transrectal prostate biopsy performed for elevated serum

In the present study, a case-control association study was conducted with the specific aims of identifying and confirming both genetic and non-genetic risk factors

Spindle cell squamous cell carcinoma was excluded because of the negative results for pan-CK, p63, and CK 5/6; malignant melanoma was excluded by the negative results