• Journal of Korean Neurosurgical Society
• /
• 제64권2호
• /
• pp.316-319
• /
• 2021

Extramedullary plasmacytoma and solitary plasmacytoma are localized neoplasms. Solitary plasmacytoma of bone consists about 4% of malignant plasma cell tumors. A plasmacytoma involving the frontal bone is unusual, and a limited number of cases have been reported. We present a rare case of a solitary plasmacytoma of the frontal bone manifesting as a forehead lump.

• Journal of the Korean Association of Oral and Maxillofacial Surgeons
• /
• 제32권3호
• /
• pp.235-240
• /
• 2006

Solitary plasmacytoma is a rare malignant neoplasm that originate in immunoglobulin-producing plasma cell. Solitary bone plasmacytoma can be found at any site throughout the skeleton and in most cases eventually progresses to multiple myeloma, of which it is thought to be an unusual presentation. On the other hand, extramedullary plasmacytoma has a tendency to occur in the head and neck region, mainly in association with the upper air passages. Incisional biopsy is the primary approach to make a definitive diagnosis, and immunohistochemical staining can be very helpful in understanding the nature of these tumors. We report a 66 years old patient with solitary bone plasmacytoma and a 36 years old patient with solitary extramedullary plasmacytoma with literatures review.

• Journal of Korean Neurosurgical Society
• /
• 제46권2호
• /
• pp.156-160
• /
• 2009

Solitary extramedullary plasmacytomas are isolated plasma cell tumors of soft tissue that typically do not metastasize. They are rare and account for 4% of all plasma cell tumors. To our knowledge, only 14 cases of solitary extramedullary plasmacytomas in the sphenoid sinus have been reported. A 32-year-old man presented to our department with complaint of ocular pain in the right eyeball and diplopia. Physical and neurological examinations revealed intact and prompt direct and indirect light reflexes in both pupils and limitation of extraocular muscle movement seen with the lateral gaze of the right eyeball. Magnetic resonance imaging suggested the presence of mucocele or mycetoma, therefore surgical resection was performed with endoscopic endonasal transsphenoidal approach. Histopathology was consistent with plasmacytoma. Systemic work-up did not show any evidence of metastasis and the sphenoid sinus was the sole tumor site, and therefore the diagnosis of solitary extramedullary plasmacytoma was confirmed. We report a rare case of solitary extramedullary plasmacytoma in the sphenoid sinus with successful treatment using the endoscopic endonasal transsphenoidal resection and adjuvant radiotherapy.

• Journal of Chest Surgery
• /
• 제46권6호
• /
• pp.482-485
• /
• 2013

Plasmacytoma is a plasma cell neoplasm that locally infiltrates a bone or spreads to extramedullary areas. A new World Health Organization criterion defines solitary plasmacytoma of bone as a localized bone tumor consisting of plasma cells identical to those seen in plasma cell myeloma, which is manifested as a solitary osteolytic lesion in a radiological evaluation. Primary tumors of the sternum are generally malignant, and solitary plasmacytomas of the sternum are very rare tumors. We present herein the case of a patient who had a primary sternal tumor with solitary plasmacytoma and no evidence of multiple myeloma.

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

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

• 한국임상수의학회지
• /
• 제29권4호
• /
• pp.356-359
• /
• 2012

암컷, 8년령, 3.2 kg의 시츄견이 간헐적인 구토를 주증으로 내원하였다. 기본 혈액검사 및 방사선 검사에서 특별한 이상 소견은 관찰되지 않았다. 복부 초음파 검사에서 위벽에서 유래한 것으로 생각되는 저에코의 둥근 종괴가 관찰되었다. 위 내시경 검사에서 둥근 종괴가 유문동 벽에서 내강으로 돌출되어 있고, 종괴 및 주변 점막의 비정상적인 소견은 관찰되지 않았다. 이에 위 종괴 절제술을 실시하였고, 면역 염색을 포함한 조직학적 검사에서 extramedullary plasmacytoma로 진단되었다. 환자는 임상 증상이 개선되었으며, 약 2년 동안 재발 및 전이 소견 없이 건강한 상태이다.

• Asian Pacific Journal of Cancer Prevention
• /
• 제16권9호
• /
• pp.3741-3745
• /
• 2015

Background: A moderate dose of radiation is the recommended treatment for solitary plasmacytoma (SP), but there is controversy over the role of surgery. Our study aimed at comparing different treatment modalities in the management of SP. Materials and Methods: Data from 38 consecutive patients with solitary plasmacytoma, including 16 with bone plasmacytoma and 22 with extramedullary plasmacytoma, were retrospectively reviewed. 15 patients received radiotherapy alone; 11 received surgery alone, and 12 received both. The median radiation dose was 50Gy. All operations were performed as radical resections. Local progression-free survival (LPFS), multiple myeloma-free survival (MMFS), progression-free survival (PFS) and overall survival (OS) were calculated and outcomes of different therapies were compared. Results: The median follow-up time was 55 months. 5-year LPFS, MMFS, PFS and OS were 87.0%, 80.9%, 69.8% and 87.4%, respectively. Univariate analysis revealed, compared with surgery alone, radiotherapy alone was associated with significantly higher 5-year LPFS (100% vs 69.3%, p=0.016), MMFS (100% vs 51.4%, p=0.006), PFS (100% vs 33.7%, p=0.0004) and OS (100% vs 70%, p=0.041). Conclusions: Radiotherapy alone can be considered as a more effective treatment for SP over surgery. Whether a combination of radiotherapy and surgery improves outcomes requires further study.

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

• Maxillofacial Plastic and Reconstructive Surgery
• /
• 제29권1호
• /
• pp.85-90
• /
• 2007

Plasma cell neoplasms are generally categorized into four groups; multiple myeloma(MM), solitary plasmacytoma of the bone(SPB), plasma cell leukemias, and extramedullary plasmacytomas(EMP). These tumors may be further described as localized or diffuse in presentation. Localized plasma cell neoplasms are rare occurrences and include solitary plasmacytomas of the skeletal system, which account for 2-5% of all plasma cell neoplasms and extramedullary plasmacytomas of the soft tissue, which account for approximately 3% of all such neoplasms. A plasmacytoma is defined as any discrete, most likely solitary mass of neoplastic plasma cells either in the bone marrow or in various soft tissue sites. Diffuse lesions include the other two groups, multiple myeloma and plasma cell leukemia. The relationship between these processes has not yet been definitively characterized, but there appears to be a continuum in which both SPB and EMP often progress to MM. The patient was referred who had continuous deep throbbing bone pain and swelling on the left posterior gingival area of the mandible after extraction of the first and second molar. The result of intraoperative excisional biopsy of the lesion was confirmed as a plasmacytoma. And it revealed systemic multiple myeloma through the further diagnostic work-up. It is worth to report because of a rare case of multiple myeloma found in oral cavity as a form of plasmacytoma.