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Incidental and Isolated Follicular Lymphoma In Situ and Mantle Cell Lymphoma In Situ Lack Clinical Significance.

偶发及孤立的原位滤泡淋巴瘤及原位套细胞细胞淋巴瘤并无临床意义

Bermudez G,González de Villambrosía S,Martínez-López A,Batlle A,Revert-Arce JB,Cereceda Company L,Ortega Bezanilla C,Piris MA,Montes-Moreno S

Abstract

Follicular lymphoma in situ (FLIS) and mantle cell lymphoma in situ (MCLIS) are histopathologic findings of undetermined clinical significance. We studied a series of 341 consecutive lymph node resection specimens from patients diagnosed with colorectal (201 cases) and breast (140 cases) adenocarcinoma between 1998 and 2000. Incidental and isolated FLIS was identified in 11/341 patients (3.23%), whereas incidental and isolated MCLIS was found in 2/341 patients (0.59%). None of these cases developed overt lymphoma. A second series of 17 cases of FLIS (16 cases) and MCLIS (1 case) from consultation files was analyzed. Five cases with incidental and isolated FLIS were identified. None of these cases developed overt lymphoma. Overall, none of the 16 cases with incidental and isolated FLIS in both series developed overt FL after a median follow-up of 54 months (range, 7 to 187 mo). However, 12 of these cases with a clinical suspicion of lymphoproliferative disorder showed the association (in different lymph nodes) or combination (in the same sample) of FLIS or MCLIS with other lymphoid neoplasms (FL, splenic marginal zone lymphoma, nodal marginal zone lymphoma, Hodgkin lymphoma, diffuse large B-cell lymphoma, chronic lymphocytic leukemia/small lymphocytic lymphoma, multiple myeloma). In conclusion, the clinical relevance of FLIS and MCLIS seems to strictly depend on the clinical context. Incidental FLIS or MCLIS seem to have a very low risk for transformation, which recommends careful clinical examination after histopathologic diagnosis and conservative management with follow-up for a limited period of time.

摘要

原位滤泡性淋巴瘤(FLIS)及原位套细胞淋巴瘤(MCLIS)是组织病理学的诊断产物,其临床意义不明。

我们研究了自1998年至2000年期间所诊断的341例结直肠癌(201例)及乳腺癌(140例)患者的连续淋巴结切除标本。11/341(3.23%)例患者被确认为偶发及孤立FLIS,2/341(0.59%)例患者为偶发及原位MCLIS。这些患者都未发展为明显的淋巴瘤。

另外研究了17例(FLIS 16例,MCLIS 1例)会诊病例。5例为偶发及孤立FLIS。这些病例均未发展为明显的淋巴瘤。

中位随访54个月后(7-187个月),这16例FLIS病例均未发展为滤泡性淋巴瘤。

然而,在这些病例中,12例临床怀疑为淋巴增殖性疾病,表现为与其他淋巴样肿瘤(包括滤泡性淋巴瘤、脾边缘区淋巴瘤、结内边缘区淋巴瘤、霍奇金淋巴瘤、弥漫大B细胞淋巴瘤、慢性淋巴细胞性白血病/小淋巴细胞性淋巴瘤及多发性骨髓瘤)相关(在不同的淋巴结)或相结合(在相同的淋巴结)。FLIS及MCLIS的临床意义应该严格依据于临床实践。偶发FLIS及MCLIS向淋巴瘤转化风险较低,这要求临床医生在病理诊断该组疾病后进行详细的检查、保守治疗及规定时间随访。

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