Buradasınız

Castleman hastalığı (Supraklavikular lokalizasyonlu giant lenf nodu hiperplazisi)

Castleman's disease (A giant lymph node hyperplasia at supraclavicular region)

Journal Name:

Publication Year:

Keywords (Original Language):

Abstract (2. Language): 
('astleman \s Disease, also known as giant lymph node hyperplasia, is a benign lymphoproliferatife disorder. 2/3 of the cases shows mediastinal and pulmonary involvement, 13 shows extramediastinal lymph node and extra nodal involvement. Histologically, hyaline vascular (HI' type, % 90), plasma cell (PC type % 10) and mixed types were identijied. This case was diagnosed by supraclavicular lymph node biopsy ( PC type). Because of its unusual localization and rare histologic tyjx, we evaluated the literature and reported the case. [Journal of Turgut Özal Medical Center 1(2): 149-153, 1994f
Abstract (Original Language): 
Castleman hastalığı (CD) (Hani Lenf Nodu Hiperplazisi (GLNH) de denen benign lenfoprolifer atıfbir hastalıktır. Olguların 2 3'ü mediasten ve pulmoner tutulum, 13u mediasten dışı lenf nodları ve ekstranodal tutulum gösterir. Histolojik olarak hiyalin vasküler tip (fil ' tip. % 90), plazma hücreli tip (PC tip. % 10) ve çok daha nadir görülen miLst tip olmak üzere 3 tip tanımlanmıştır. Supraklavikular lenf nodu biopsisı ile CD (PC tip) tanısı koyduğumuz olgumuzu hem lokalizasyon hem de histolojik tip olarak nadir rastlanması nedeniyle sunduk ve bu konuda literatür araştırdık.[Turgut Özal Tıp Merkezi Dergisi 1(2): 149¬153. 1994]
149-153

REFERENCES

References: 

1. Baruch Y, Ben-Arie Y, Kerner H, et al. Giant lymph node hyperplasia (Castleman's disease): a clinical study of eight patients. Postgrad Med J 1991; 67:366-70.
2. Kimura H, Watanabe Y, Ohashi N, at al. Immunologic study of the hyaline-vascular type of Castleman's disease a case study. Acta Otolaryngol (Stockh) suppl 1993; 504:146-50.
3. Penfold CN, Cottrell BJ, Talbot R. Neonatal giant lymph node hyperplasia (Castleman disease) presenting in the head and neck. Brit J Oral & Maxillofacial Surg 1991; 29: 110-1.
4. Loftus MJ, Ford CN, Hafez GR, et al. Pathologic quiz case 1, Pathologic quiz case 2, Arch Otolaryngol Head Neck Surg 1991; 117:224-6.
5. Reynolds SP, Gibbs AR, Weeks H, Davies BH. Massive pleural effusion: an unusual presantation of Castleman's disease. Eur Respir J 1992;5:1150-3.
6. Massey GT, Konstein MJ, Wahl D, et al. Angiofollicular Lymph Node Hyperplasia (Castleman's disease) in an adolescent female. Clinical and Immunologic Findingis. Cancer 1991;68:1365-72.
7. Sherman D, Ramsay B, Theodorou NA, et al. Reversible plane xanthoma, vasculitis and peliosis hepatis in giant lymph node hyperplasia (Castleman's disease): A case of report and review of the cutaneous manifestations of giant lymph node hyperplasia. J Am Acad Dermatol 1992;26:105-9.
8. Wolf M, Kessler A, Horovitz A. Benign angiofollicular lymph node hyperplasia (Castleman's disease). Oral Maxillofac Surg 1991 ;49:1129-31.
9. Velde G, Thunnissen FBJM. Anterior mediastinal tumor of 30 years duration. Chest 1992;100:869-70.
10. Ravet LB, Peuchmaur M, Devergne O, et al. Interleukin-6 Gene Expression in Castleman's disease. The Am Soc Hematol 1991;2923-30.
11. Mandel C, Silberstein M, Hennessy O. Case report: fatal pulmonary Kaposi's sarcoma and Castleman's disease in a renal transplant recipient Brit J Radiol 1993.66: 264-5. 12 Ruco LP, Gearing AJH, Pigott R, et al Expression of ICAM-1, VCAM-1 and ELAM-1 in angiofollicular lymph node hyperplasia (Castleman's disease): evidence for dysplasia of follicular dentritic reticulum cells. Histopathology 1991;19:523-8.

Thank you for copying data from http://www.arastirmax.com