1.Plasma Cell Granuloma Associated with Pulmonary Actinomycosis: A Case Report.
Seoung Ju PARK ; Yong Chul LEE ; Yang Keun RHEE ; Eui Yong KWEON ; Heung Bum LEE
Journal of Korean Medical Science 2006;21(6):1117-1120
Plasma cell granuloma (PCG) of the lung is a rare disease that usually presents as a pulmonary nodule or mass on incidental radiographic examination without symptoms. Although the etiology of PCG is still controversial, many findings have lent support to the lesion being a reactive inflammatory process rather than a neoplastic one. We describe a 53-yr-old male who presented with a hemoptysis and have a lung mass at the left upper lobe on chest radiograph. The lung mass was primarily diagnosed as PCG by percutaneous needle aspiration and biopsy, and the patient was treated with oral steroid because he and relatives refused the operation. However, the size of the lung mass did not change and open thoracotomy and lobectomy were done therefore. He was confirmed as having pulmonary actinomycosis with PCG after surgery. To our knowledge, this is the first report of PCG associated with actinomycosis in Korea.
Middle Aged
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Male
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Lung Diseases/*complications/*diagnosis
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Humans
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Granuloma, Plasma Cell/*complications/*diagnosis
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Actinomycosis/*complications/*diagnosis
2.Fever of Unknown Origin as a Presentation of Gastric Inflammatory Myofibroblastic Tumor in a Two-Year-Old Boy.
Min Young CHO ; Youn Ki MIN ; Nam Ryeol KIM ; Seong Jin CHO ; Han Kyeom KIM ; Kwang Chul LEE ; Sung Ock SUH ; Cheung Wung WHANG
Journal of Korean Medical Science 2002;17(5):699-703
Gastric inflammatory myofibroblastic tumor (IMT) is an extremely rare lesion with mimicking malignant features and accompanied with various clinical manifestations. Here we present a 2-yr-old boy who had a gastric IMT with a huge extragastric mass, which closely resembled a neuroblastoma on imaging studies. He experienced intermittent fever and poor appetite for 6 weeks. Fever remained up to 38degrees C even on the operation day. He underwent partial gastrectomy and distal pancreatectomy with splenectomy including the tumor. The preoperative fever disappeared and did not recur in the postoperative course.
Child, Preschool
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Fever of Unknown Origin/*etiology
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Granuloma, Plasma Cell/*complications/*diagnosis/surgery
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Humans
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Male
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Stomach Diseases/*complications/*diagnosis/surgery
3.A Case of Hepatic Inflammatory Pseudotumor Developed with Peripheral Cholangiocarcinoma.
Hyun Woong LEE ; Byoung Kuk JANG ; Woo Jin CHUNG ; Kyung Sik PARK ; Kwang Bum CHO ; Jae Seok HWANG ; Yu Na KANG ; Koo Jeong KANG ; Jung Hyeok KWON
The Korean Journal of Gastroenterology 2006;48(3):200-204
Inflammatory pseudotumor is an uncommon mass which develops most frequently in the lung of young adults. It is characterized by localized fibrous proliferations with chronic inflammatory cell infiltration. Due to its rarity and similarity in radiologic appearance with malignant hepatic tumors, hepatic inflammatory pseudotumor (HIPT) is often misdiagnosed and resected accidentally. We report a case of HIPT which was unnecessarily resected due to synchronous small peripheral cholangiocarcinoma located on the other segment of liver.
Bile Duct Neoplasms/complications/*diagnosis/pathology
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*Bile Ducts, Intrahepatic
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Cholangiocarcinoma/complications/*diagnosis/pathology
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Fatal Outcome
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Granuloma, Plasma Cell/complications/*diagnosis/pathology
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Humans
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Liver Diseases/complications/*diagnosis/pathology
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Male
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Middle Aged
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Tomography, X-Ray Computed
4.Inflammatory Myofibroblastic Tumor on Intercostal Nerve Presenting as Paraneoplastic Pemphigus with Fatal Pulmonary Involvement.
Dong Hyun LEE ; Sun Ho LEE ; Joo Kyung SUNG
Journal of Korean Medical Science 2007;22(4):735-739
Inflammatory myofibroblastic tumors (IMTs) are benign neoplasms that can occur at different anatomic sites with nonspecific clinical symptoms. A 48-yr-old woman presented with a 2-month history of a relapsed oral ulcer, progressive dyspnea, and a thoracic pain induced by breathing. A tumorous mass was noticed in the right costodiaphragmatic recess on chest computed tomography and magnetic resonance imaging, and the patient underwent a right costotransversectomy with excision of the tumor, which originated from the 12th intercostal nerve. Histology and immunohistochemistry showed that the tumor was an IMT of the intercostal nerve. The patient's postoperative course was not favorable; dyspnea persisted after surgery, and a progressive pulmonary compromise developed. The cause of the respiratory failure was found to be bronchiolitis obliterans, which in this case proved to be a fatal complication of paraneoplastic pemphigus associated with an IMT. This case of IMT of the spinal nerve in the paravertebral region is unique in terms of its location and presentation in combination with paraneoplastic pemphigus, which is rare. A brief review of the heterogeneous theories concerning the pathogenesis, clinicopathological features, and differential diagnosis of this disease entity is presented.
Diagnosis, Differential
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Fatal Outcome
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Female
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Granuloma, Plasma Cell/complications/*pathology
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Humans
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Intercostal Nerves/*pathology
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Lung Diseases/etiology/pathology
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Middle Aged
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Paraneoplastic Syndromes/etiology/*pathology
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Pemphigus/etiology/*pathology
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Peripheral Nervous System Neoplasms/complications/*pathology