The gut-associated lymphoid tissues are the guardians of the enteric immune system and integrate dietary and microbial stimuli to maintain immunologic tolerance. However, during periods of persistent chronic inflammation, such as in Crohn’s disease (CD), a dysfunctional lymphatic system is a pathologic hallmark. Indeed, the predominant histopathologic features of CD are lymphocytic lymphangitis, occluded lymphatic vessels, and inflammatory granulomas. These trademark features of chronic disease are found in or around ectopic tertiary lymphoid tissues (TLT) in the inflamed lamina propria (Gut 2008;57:1-4). In addition, the presence of TLT at the base of aphthous ulcers is the earliest endoscopically evident lesion in CD and their appearance heralds recurrent disease within the neoterminal ileum after ilectomy (Gut 1984;25:665-672). To date, the function of intestinal TLT and their impact on the etiology and pathogenesis of CD remains enigmatic, with limited experimental evidence as to their role. How TLT integrate into the pathophysiology of CD remains a critical question, yet clinical investigation into their development and function remains limited. Randolph et al aimed to assess the integrity of mesenteric lymphatic vasculature in CD. First, they confirmed the previous findings generated from immunopathologic studies of intestinal mucosa, indicating defective lymphatic function during active disease. To achieve this, patent blue dye was injected into the serosa of ileal loops before surgical resection, highlighting afferent lymphatic vessels draining the lamina propria. This technique nicely demonstrated a deviation of normal lymphatic vessels in active CD, compared with non-CD counterparts and indicated a remodeling of the vasculature in the mesentery. Next, they used a 3-dimensional system to image whole mount sections from a patient cohort undergoing ilectomy for stricturing CD (to obtain cm3 tissue coverage). Surprisingly, this work revealed advanced remodeling of the lymphatic vascular tracks, with the presence of ectopic lymphoid follicles within the collecting vessel line. A border of adipocytes and no evident capsule, suggesting that these organized structures were not sentinel lymph nodes but TLT instead. The work by Randolph et al highlights that, although most studies have reported on lymphatic capillaries in the intestinal wall, where collecting vessels remove solutes and immune cells, the primary functional site of lymphatic dysfunction may be the larger vessels in the mesentery, which interface with sentinel lymph nodes.