Sachdev Ritesh, Setia Namrata, Jain Shyama
Department of Pathology, Maulana Azad Medical College, New Delhi, India.
Med Oral Patol Oral Cir Bucal. 2007 May 1;12(3):E198-200.
Sinus histiocytosis with massive lymphadenopathy (SHML) is a benign proliferating histiocytic disorder, predominantly of lymph nodes with extra-nodal involvement in some cases. It is a self-limiting disease and has a good prognosis; however some patients need steroid therapy. Therein lays a need to differentiate it from other lympho proliferative disorders of poorer prognosis. Clinically, it is suspected only when there is a significant lymph node enlargement in younger age group as the term signifies. Recently, we came across a case where a middle-aged female presented with a subtle swelling in submental region, clinically suspected of reactive or tubercular etiology. However on fine needle aspiration cytology, the smears showed many histiocytes, some of them showing lymphocytes and plasma cells in their cytoplasm, a morphological feature called as "emperipolesis" classically seen in SHML. The present case is reported because of unusual clinical presentation and possibly the need for a revision of existing terminology.
伴巨大淋巴结病的窦性组织细胞增生症(SHML)是一种良性增生性组织细胞疾病,主要累及淋巴结,部分病例有结外受累。它是一种自限性疾病,预后良好;然而,一些患者需要类固醇治疗。因此,有必要将其与其他预后较差的淋巴增生性疾病区分开来。临床上,仅当较年轻年龄组出现明显淋巴结肿大时才会怀疑该病,正如该术语所表示的那样。最近,我们遇到一例中年女性,其颏下区域有轻微肿胀,临床上怀疑为反应性或结核性病因。然而,细针穿刺细胞学检查涂片显示有许多组织细胞其中一些在细胞质中含有淋巴细胞和浆细胞,这是一种在SHML中经典可见的形态学特征,称为“血细胞吞噬现象”。报告本病例是因为其临床表现不寻常,可能需要对现有术语进行修订。