• Maxillofacial Plastic and Reconstructive Surgery
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• 제18권1호
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• pp.109-114
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• 1996

수질의 형질세포종(extramedullary plasmacytoma)은 극히 드물게 나타나는 형질세포 악성종양(plasma cell malignancy)중 하나이며 치은에 발생한 경우는 거의 보고된바 없다. 다발성 골수종과의 감별진단은 조직학적 검사 후에도 여러 혈액검사 및 병이화학 검사가 필요하며 초기진단에 확실한 검사는 어렵다. Pahor등에 의하면 수질외 형질세초종의 5년생존률이 60%인 것에 비해 다발성 골수종에서는 5.7%를 보여 예후에 있어서 현저한 차이를 보이고 보든 수질외 형질세포종환자에 있어서 전신질환으로의 진행 가능성은 배제할 수 없으므로 장기간의 관찰이 필수적이라고 할 수 있다. 저자 등은 신장이식 수술 후 면역억제제를 사용한 15세 환자에서 치은에 발생한 형질세포을 치험하였기에 문헌 고찰과 함께 진단, 예후, 치료 및 면역 억제제와의 연관성에 관하여 보고하는 바이다.

• Radiation Oncology Journal
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• 제3권1호
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• pp.35-39
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• 1985

Solitary Extramedullary plasmacytoma는 plasma cell neoplasm중 드문 것으로 다른 형태의 plasmacytoma와는 임상적 명리학적으로 완전히 다른 종양으로 알려져 있다. 원발병소는 주로 두경부 특히 상기도로써 주로 국소부위에 발생하며, 국소방사선치료가 근본적 치료로 받아들여지고 있다. 저자들은 1970년 1월부터 1984년 12월까지 두 경부의 solitary Extramedullary Plasmacytoma로 확진되어 연계암센터 방사선 치료실에서 방사선 치료를 받았던 5예를 대상으로 추적 조사하여 그 결과를 보고하는 바이다. 전 5예 모두 진단당시 국소부위에 단일 템소를 갖고 있였고 이중 1예에서 원발병소에 수술을 시행하였으나 수술 후 국소재발이 있었고 곧 전신으로 퍼졌으며 진단 후 3년 6개월만에 사망하였다. 나머지 4예중 2예에서는 방사선치료만 시행하였고 다른 2예에서는 수술 및 수술 후 방사선 치료를 시행하였는데 4예 모두 현재까지 병변없이 생존하고 있다.

• 한국임상수의학회지
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• 제41권1호
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• pp.18-23
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• 2024

A 13-year-old spayed female Golden Retriever with clinical signs of weight loss and lethargy presented with two esophageal masses and one sessile polyp on computed tomography and esophagoscopy. Endoscopic snare resection was performed, and histopathological examination was requested. Based on histopathology and immunohistochemistry of multiple myeloma oncogene 1 staining, the patient was diagnosed with esophageal extramedullary plasmacytoma. The patient remained clinically well without any clinical signs during a follow-up period of 12 months. Herein, we report the successful diagnosis and management of esophageal extramedullary plasmacytoma in a dog using endoscopy.

• Journal of Korean Neurosurgical Society
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• 제29권5호
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• pp.701-705
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• 2000

Solitary plasmacytomas are rare and account for 5-10% of all plasma cell disorders. These tumors are categorized as solitary plasmacytomas of bone(osseous) or extramedullary plasmacytomas(non-osseous). About a half of solitary plasmacytomas of bone occur in the spine but rarely in the skull. We report a case of solitary plasmacytoma of the skull presented with a painless palpable left parietal calvarial mass in an otherwise asymptomatic 38- year-old man. Skull radiographs showed a large radiolucent lesion with well defined non-sclerotic margins. Computed tomograph scan demonstrated a markedly enhancing mass extending from the epidural to the subcutaneous space. The patient underwent surgery and tumor was completely excised. Pathological examination showed tumor to be a plasmacytoma synthesizing IgG. Postoperatively, the patient received radiotherapy. There was no evidence of systemic involvement on postoperative laboratory wokups. Our recommended treatment is a complete surgical excision combined with postoperative radiation therapy. The patient should be follwed carefully for more than 10 years because of either local recurrence or possible progression to multiple myeloma.

• Tuberculosis and Respiratory Diseases
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• 제78권3호
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• pp.262-266
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• 2015

Plasmacytomas are extramedullary accumulations of plasma cells originating from soft tissue. Mediastinal plasmacytoma is a rare presentation. A 67-year-old man recovered after antibiotic treatment for community-acquired pneumonia. However, on convalescent chest radiography after 3 months, mass like lesion at the right lower lung field was newly detected. Follow-up chest computed tomography (CT) revealed an increase in the extent of the right posterior mediastinal mass that we had considered to be pneumonic consolidations on previous CT scans. Through percutaneous needle biopsy, we diagnosed IgG kappa type extramedullary plasmacytoma of the posterior mediastinum.

• Journal of Yeungnam Medical Science
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• 제31권1호
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• pp.43-47
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• 2014

Extramedullary plasmacytoma (EMP) is a rare disease that occurs in 3% to 5% of patients with plasma cell disorder. It occurs most commonly in the upper respiratory tract and the oral cavity. Very few EMP cases have been reported in the central nervous system (CNS). We report herein an unusual case of EMP in the nasal cavity that recurred in the CNS without systemic involvement. A 67-year-old man visited our hospital due to a month-long bout with exophthalmos. He was diagnosed with EMP in the nasal cavity, paranasal sinus, and orbital cavity. He received radiotherapy to which he had complete responses. After 2 years, he visited our hospital because of a month-long headache. He was diagnosed with EMP recurrence in the CNS via brain magnetic resonance imaging and cerebrospinal fluid analysis. He was treated with whole brain radiotherapy and intrathecal chemotherapy with methotrexate, but he expired due to pneumonia.

• 대한세포병리학회지
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• 제10권1호
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• pp.67-71
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• 1999

We report a case of 53-year-old man with plasmacytold transitional cell carcinoma of the urinary bladder, which may be confused with plasmacytoma. The patient initially presented with gross hematuria and dysuria for two months. Cystoscopy and radiologic studios revealed multiple intraluminal protruding masses on the urinary bladder invading perivesical fat tissue. After urinary cytologic examination and cystoscopic biopsy, radical cystectomy and pelvic lymph node dissections were done. Urine cytology showed single cells and poorly cohesive cells with round eccentric nuclei, bi-or multi-nucleation, indistinct nucleoli, coarse chromatin, and abundant basophilic cytoplasm within relatively clear background. The cytologic findings of tumor cells were similar to the plasma cells seen in plasmacytoma. The tumor of the bladder was composed on discohesive, individual cancer cells with diffuse pattern that simulated lymphoma or plasmacytoma. Immunohistochemical and electron microscopic studies clearly established the epithelial nature of the neoplasm. Recognition of this plasmacytoid type of transitional cell carcinoma of the urinary bladder can avoid the misdiagnosis.

• Journal of Periodontal and Implant Science
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• 제9권1호
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• pp.33.2-33.2
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• 1979

• Nuclear Medicine and Molecular Imaging
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• 제43권6호
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• pp.509-512
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• 2009

This review focuses on the clinical use of $^{18}F$-FDG PET to evaluate multiple myeloma. $^{18}F$-FDG PET is useful for diagnosis, staging of multiple myeloma and differential diagnosis of myeloma related disease such as monoclonal gammopathy of undetermined significance or plasmacytoma. For therapy response, $^{18}F$-FDG PET may be effective after chemotherapy for multiple myeloma and radiotherapy for plasmacytoma.

• 한국임상수의학회:학술대회논문집
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• 한국임상수의학회 2009년도 춘계학술대회
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• pp.297-297
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• 2009