랑게르한스세포 조직구증 20예의 병리학적 특징과 Langerin (CD207)의 면역화학염색의 발현 특이성
Pathological Characteristics of 20 Cases of Langerhans Cell Histiocytosis and Specificity of Immunohistochemical Stain of Langerin (CD207)
2
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
Background : Langerhans cell histiocytosis (LCH) is a well-known neoplastic disorder of Langerhans cells which has characteristic findings, however, LCH has not been adequately studied in Korea. Methods : We analyzed the clinicopathologic features of 20 patients with LCH who were diagnosed between 1997 and 2006 at the Korea University Guro and Anam Hospitals. Results : The M:F ratio was 3:1 and the age ranged from 2-60 years (mean, 23.8 years [4 in 1st decade, 6 in 2nd decade, 2 in 3rd decade, 5 in 4th decade and 3≥40 years of age). The cases were classified as unifocal unisystemic in 13 patients, multifocal unisystemic in 4 patients, and multifocal multisystemic in 3 patients. The bone was the most commonly involved organ (14), followed by lymph node (5), lung (2), skin (2) and ureter (1). The Langerhans cells were immunohistochemically stained with Langerin, CD1a, S-100 protein, and CD68. Langerin and CD1a were specific for Langerhans cells. Conclusions : The distribution of the involved organs in patients with LCH was similar to the distribution in Western countries,but lymph node involvement was more frequent, whereas lung involvement was less common. Langerin is considered to be a specific marker for Langerhans cells.
Abstract
Background : Langerhans cell histiocytosis (LCH) is a well-known neoplastic disorder of Langerhans cells which has characteristic findings, however, LCH has not been adequately studied in Korea. Methods : We analyzed the clinicopathologic features of 20 patients with LCH who were diagnosed between 1997 and 2006 at the Korea University Guro and Anam Hospitals. Results : The M:F ratio was 3:1 and the age ranged from 2-60 years (mean, 23.8 years [4 in 1st decade, 6 in 2nd decade, 2 in 3rd decade, 5 in 4th decade and 3≥40 years of age). The cases were classified as unifocal unisystemic in 13 patients, multifocal unisystemic in 4 patients, and multifocal multisystemic in 3 patients. The bone was the most commonly involved organ (14), followed by lymph node (5), lung (2), skin (2) and ureter (1). The Langerhans cells were immunohistochemically stained with Langerin, CD1a, S-100 protein, and CD68. Langerin and CD1a were specific for Langerhans cells. Conclusions : The distribution of the involved organs in patients with LCH was similar to the distribution in Western countries,but lymph node involvement was more frequent, whereas lung involvement was less common. Langerin is considered to be a specific marker for Langerhans cells.
참고문헌 (22)
- Jaffe ES, "Pathology and genetics of tumours of haematopoietic and lymphoid tissues. World Health Organization classification of tumor", pp.280~282 (2001), IARCPress
- Ghadially FN, "Ultrastructural pathology of the cell and matrix", pp.1218~1223 (1997), Butterworth-Heinemann
- Coppes-Zantinga A, "The Langerhans cell histiocytosis X files revealed", Br J Haematol, 116, pp.3~9 (2002)
- Lichtenstein L, "Histiocytosis X: integration of eosinophilic granuloma of bone, Letterer-Siwe disease and Schuller-Christian disease as related manifestations of a single nosologic entity", AMA Arch Pathol, 56, pp.84~102 (1953)
- Nezelof C, "Histiocytosis X histogenic arguments for a Langerhans’ cell origin", Biomedicine, 18, pp.365~371 (1973)
- Nicholson HS, "The epidemiology of Langerhans cell histiocytosis", Hematol Oncol Clin North Am, 12, pp.379~384 (1998)
- Arico M, "Langerhans cell histiocytosis in adults: report from the International Registry of the Histiocyte Society", Eur J Cancer, 39, pp.2341~2348 (2003)
- Hoover KB, "Langerhans cell histiocytosis", Skeletal Radiol, 36, pp.95~104 (2007)
- Willis B, "Disease course and late sequelae of Langerhans’ cell histiocytosis:25-year experience at the University of California, San Francisco", J Clin Oncol, 14, pp.2073~2082 (1996)
- Bernstrand C, "Long-term followup of Langerhans cell histiocytosis: 39 years’ experience at a single centre", Acta Paediatr, 94, pp.1073~1084 (2005)
- Yang WI, "Immunohistochemical study on antigenic phenotype of Langerhans cell histiocytosis", Yonsei Med J, 33, pp.309~319 (1992)
- Lyu GS, "Cytologic features of Langerhan’s cell histiocytosis", Korean J Cytopathol, 2, pp.153~159 (1991)
- Sung SH, "Infantile solitary eosinophilic granuloma of the lymph node: a case report", Korean J Pathol, 26, pp.277~282 (1992)
- Valladeau J, "Langerin, a novel C-type lectin specific to Langerhans cells, is an endocytic receptor that induces the formation of Birbeck granules", Immunity, 12, pp.71~81 (2000)
- Hunger RE, "Langerhans cells utilize CD1a and Langerin to efficiently present nonpeptide antigens to T cells", J Clin Invest, 113, pp.701~708 (2004)
- Mizumoto N, "CD1a and Langerin: acting as more than Langerhans cell markers", J Clin Invest, 113, pp.658~660 (2004)
- Lee JH, "Unusual recurrence in ureters and maxillary sinus of Langerhans cell histiocytosis involving mastoid bone", Pathol Res Pract, 200, pp.845~849 (2005)
- Pileri SA, "Tumours of histiocytes and accessory dendritic cells: an immunohistochemical approach to classification from the International Lymphoma Study Group based on 61 cases", Histopathology, 41, pp.1~29 (2002)
- Howarth DM, "Langerhans cell histiocytosis: diagnosis, natural history, management, and outcome", Cancer, 85, pp.2278~2290 (1999)
- Donato R, "Intracellular and extracellular roles of S100 proteins", Microsc Res Tech, 60, pp.540~551 (2003)
- Lau SK, "Immunohistochemical expression of Langerin in Langerhans cell histiocytosis and non-Langerhans cell histiocytic disorders", Am J Surg Pathol, 32, pp.615~619 (2008)
- Dziegiel P, "Coexpression of CD1a, langerin and Birbeck’s granules in Langerhans cell histiocytoses (LCH) in children: ultrastructural and immunocytochemical studies", Folia Histochem Cytobiol, 45, pp.21~25 (2007)
