Mamoon Nadira, Haroon Asna, Luqman Muhammad, Jamal Shahid
Department of Histopathology, Armed Forces Institute of Pathology, Rawalpindi.
J Coll Physicians Surg Pak. 2003 Mar;13(3):138-42.
To observe and document the clinical features, mode of presentation, histopathological and immunohistochemical features of Kikuchi's disease.
An observational and descriptive study.
Histopathology department, Armed Forces Institute of Pathology, Rawalpindi from January, 1997 to December, 2001. SUBJECTS AND METHODS Thirty-one cases of Kikuchi's disease of lymph node were diagnosed during the study period. Hematoxylin and Eosin stained slides were examined and histological features including extent of architectural effacement, zonation, extent of necrosis, and cellular composition were recorded. Special stains and immunohistochemistry was done.
Kikuchi's disease was diagnosed in 31 cases (1.9%) out of 5762 lymph node biopsies received. There were 10 male and 21 female patients. Ten patients were aged between 21 and 25 years (33%). Eight (25.8%) patients were from pediatric age group. Thirty patients (96.4%) presented with cervical lymphadenopathy. Thirteen (41.9%) lymph nodes showed fragmentation, while 8 (25.8%) revealed perinodal spill. Seventeen cases (54.7%) showed more than 50% necrosis. Zonation was seen in 13 (41.9%) cases. Immunohistochemistry showed majority of cells to be histiocytes and T-lymphocytes. Eight cases were followed-up, all of which showed regression of symptoms over 4-8 months.
Kikuchi's disease is an uncommon cause of cervical lymphadenopathy in young females. Necrotic areas, karyorrhexis, zonation, absence of neutrophils and predominance of histiocytes with many plasmacytoid monocytes are features that aid in diagnosis. Immunohistochemistry can be used to differentiate it from malignant lymphoma. It is important for clinicians and pathologists to be aware of this entity as it is a benign disorder with a self-limiting course.
观察并记录菊池病的临床特征、表现方式、组织病理学及免疫组化特征。
一项观察性和描述性研究。
1997年1月至2001年12月,拉瓦尔品第武装部队病理研究所组织病理学部门。
在研究期间诊断出31例淋巴结菊池病。检查苏木精-伊红染色切片,记录组织学特征,包括结构破坏程度、分区、坏死程度及细胞组成。进行特殊染色和免疫组化检测。
在收到的5762例淋巴结活检中,31例(1.9%)诊断为菊池病。男性10例,女性21例。10例患者年龄在21至25岁之间(33%)。8例(25.8%)患者来自儿童年龄组。30例(96.4%)表现为颈部淋巴结病。13例(41.9%)淋巴结显示碎裂,8例(25.8%)有结周外溢。17例(54.7%)显示坏死超过50%。13例(41.9%)可见分区。免疫组化显示大多数细胞为组织细胞和T淋巴细胞。8例进行了随访,所有病例在4至8个月内症状均消退。
菊池病是年轻女性颈部淋巴结病的罕见病因。坏死区域、核碎裂、分区、无中性粒细胞以及以许多浆细胞样单核细胞为主的组织细胞占优势是有助于诊断的特征。免疫组化可用于将其与恶性淋巴瘤鉴别。临床医生和病理医生了解这一疾病很重要,因为它是一种具有自限性病程的良性疾病。