Lymphoglandular Complex-Like Colorectal Carcinoma—A Series of 20 Colorectal Cases, Including Newly Reported Features of Malignant Behavior

Author:

Yilmaz Osman12,Westerhoff Maria3,Panarelli Nicole4,Hart John5,Groisman Gabriel6,Ruz-Caracuel Ignacio7,Loughrey Maurice8,Matsukuma Karen9,Lee Soo Hyun10,Yilmaz Omer11,Gonzalez Raul S.12,Deshpande Vikram12

Affiliation:

1. Department of Pathology, Beth Israel Deaconess Medical Center

2. Harvard Medical School, Boston, MA

3. Department of Pathology, University of Michigan, Ann Arbor, MI

4. Department of Pathology, Montefiore Albert Einstein College of Medicine, New York, NY

5. Department of Pathology, University of Chicago, Chicago, IL

6. Department of Pathology, Hillel Yaffe Medical Center, Hadera, Israel

7. Department of Pathology, Hospital Universitario Ramon y Cajal, IRYCIS, CIBERONC, Madrid, Spain

8. Department of Pathology, Royal Victoria Hospital Belfast Trust, Belfast, N. Ireland

9. Department of Pathology, University of California Davis, Sacramento, CA

10. Department of Pathology, Boston University Medical Center

11. Department of Pathology, Massachusetts General Hospital, Boston, MA

12. Department of Pathology, Emory University, Atlanta, GA

Abstract

Distinguishing colon carcinoma that is surrounded by well-circumscribed lymphoid tissue from adenomas involving lymphoglandular complexes can be difficult. We assessed a multi-institutional international cohort of 20 colorectal carcinomas with associated prominent lymphoid infiltrates, which we referred to as lymphoglandular complex-like carcinoma (LGCC). We collected clinical and endoscopic features, including lesion size, endoscopic appearance, location, procedure, follow-up, AJCC stage, and mismatch repair status. We recorded the presence of the following histologic features: haphazard gland distribution, gland angulation, gland fusion, solid nest formation, single-cell formation, stromal desmoplasia, presence of lymphovascular invasion and perineural invasion, presence of lamina propria, cytologic atypia as low- or high-grade, presence of goblet cells in the invasive component, and the presence of a surface lesion. Most cases (9 of 13) were described endoscopically as sessile polyps with an average size of 1.56 cm. Most cases (90%) were associated with a surface lesion, of which the majority were tubular adenomas, though a subset was associated with sessile serrated lesions with dysplasia (3 of 18). All cases of LGCC demonstrated haphazard gland distribution and either gland angulation, fusion, or solid nest formation. A portion of cases demonstrated single-cell infiltration (35%) and desmoplasia (50%), and rarely lymphovascular invasion was present (5%). A subset (10%) of cases invaded beyond the submucosa. Deficient mismatch repair was present in 22% (2 of 9) of cases for which it was performed. In cases of colectomy or completion colectomy, nodal metastasis was present in 38% (3 of 8). No cases demonstrated disease recurrence or disease-specific mortality. Overall, LGCC represents an enigmatic subset of carcinomas that is important to distinguish from adenomas involving lymphoglandular complexes due to its varying prognostic outcomes.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

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