Cerroni Lorenzo, Fink-Puches Regina, Bäck Barbara, Kerl Helmut
Department of Dermatology, University of Graz, Auenbruggerplatz 8, A-8036 Graz, Austria.
Arch Dermatol. 2002 Feb;138(2):182-9. doi: 10.1001/archderm.138.2.182.
Beginning in 1957, patients have been described with localized alopecia characterized histopathologically by mucin deposition within hair follicles (follicular mucinosis [FM]). At least 2 distinct diagnostic entities have been proposed: one occurring in children and young adults without association with other diseases ("idiopathic" FM), the other occurring in elderly patients and associated with mycosis fungoides or Sézary syndrome ("lymphoma-associated" FM).
To determine whether idiopathic and lymphoma-associated FM are distinct or related entities.
Case series.
Department of Dermatology, University of Graz, Graz, Austria.
Forty-four patients with FM were divided into 2 groups. Group 1 comprised 16 patients (mean age, 37.5 years) with no associated mycosis fungoides or Sézary syndrome; group 2 was made up of the other 28 (mean age, 52.2 years), who had clinicopathologic evidence of cutaneous T-cell lymphoma.
Mean age was lower in patients with idiopathic FM, but a considerable overlapping among the 2 groups was present. Location on the head and neck region was common in both groups, but most patients with lymphoma-associated FM had lesions also on other body sites. In fact, solitary lesions at presentation were common in patients with idiopathic FM (11 [68.8%] of 16 patients), but uncommon in those with lymphoma-associated FM (2 [7.1%] of 28 patients). Histopathologic findings did not allow clear-cut differentiation of the 2 groups. Finally, a monoclonal rearrangement of the T-cell receptor gamma gene was demonstrated by polymerase chain reaction analysis in about 50% of tested cases from each group.
Criteria previously reported to differentiate idiopathic from lymphoma-associated FM proved ineffective. In analogy to localized pagetoid reticulosis (Woringer-Kolopp disease), small-plaque parapsoriasis, and so-called solitary mycosis fungoides, idiopathic FM may represent a form of localized cutaneous T-cell lymphoma.
自1957年起,已有关于局限性脱发患者的描述,其组织病理学特征为毛囊内粘蛋白沉积(毛囊粘蛋白病[FM])。至少已提出2种不同的诊断实体:一种发生于儿童和年轻人,与其他疾病无关(“特发性”FM),另一种发生于老年患者,与蕈样肉芽肿或Sezary综合征相关(“淋巴瘤相关”FM)。
确定特发性FM和淋巴瘤相关FM是不同的还是相关的实体。
病例系列。
奥地利格拉茨医科大学皮肤科。
44例FM患者分为2组。第1组包括16例(平均年龄37.5岁)无相关蕈样肉芽肿或Sezary综合征的患者;第2组由另外28例(平均年龄52.2岁)组成,他们有皮肤T细胞淋巴瘤的临床病理证据。
特发性FM患者的平均年龄较低,但两组之间存在相当大的重叠。头颈部区域的病变在两组中都很常见,但大多数淋巴瘤相关FM患者的病变也见于身体其他部位。事实上,初发时孤立性病变在特发性FM患者中很常见(16例患者中有11例[68.8%]),但在淋巴瘤相关FM患者中不常见(28例患者中有2例[7.1%])。组织病理学检查结果无法明确区分这两组。最后,通过聚合酶链反应分析,两组中约50%的检测病例显示T细胞受体γ基因单克隆重排。
先前报道的区分特发性FM和淋巴瘤相关FM的标准被证明无效。与局限性类银屑病样网状细胞增生症(沃林格-科洛普病)、小斑块副银屑病以及所谓的孤立性蕈样肉芽肿类似,特发性FM可能代表局限性皮肤T细胞淋巴瘤的一种形式。