Dialysis patients with chronic kidney disease develop hyperphosphatemia due to their decreased capacity of phosphate excretion. Since hyperphosphatemia causes secondary hyperparathyroidism, it used to be formerly treated with aluminum agents; however, these caused problematic side effects including encephalopathy. In 2009, lanthanum carbonate was approved for coverage by Japanese health insurance. Lanthanum is assumed to be excreted from the body by secretion into bile [1]. It is known that absorbed lanthanum is deposited in the liver and bone, but since the amounts are miniscule, it had been thought not to cause organ damage. However, histopathological deposition of lanthanum has been demonstrated in the gastric mucosa [2].
Some previous reports have described various characteristics, including elevations, erosion, and ulceration [3,4,5,6,7,8,9,10, 12,13,14,15], whereas others have described the presence of whitish, rough granular mucosa [2, 11, 14,15,16,17]. Table 2 summarizes 51 cases in 13 studies that clearly describe the endoscopic findings of lanthanum deposition in the gastric mucosa, and diagnose it by biopsy. Whitish mucosa was evident in 70.6% of these cases (36/51).
Table 2 Previously reported endoscopic findings in patients with lanthanum deposition in the gastric mucosa The time from the start of lanthanum administration to histological diagnosis varied from 3 to 60 months (mean, 34.5 months). The author suggested that histologically, at least 3 months may be required for the occurrence of lanthanum phagocytosis after the start of lanthanum treatment. In previously reported cases within 12 months starting lanthanum administration with detailed endoscopic findings, whitish mucosa was evident in 83.3% (5/6) of cases in the early stage. This finding suggests that it may be an important indicator of possible lanthanum deposition in the gastric mucosa. Our retrospective review of EGD findings in the present case showed that the whitish cobblestone-like mucosa in the gastric body appeared 6 months after the start of lanthanum administration (Fig. 6).
No studies have been conducted to address the endoscopic findings of lanthanum deposition in the gastric mucosa using magnified NBI endoscopy in detail. In our patient, magnified NBI endoscopy revealed regular villous structures containing a yellowish–white substance; since this was detected below the epithelial vessels, it indicated the presence of a substance in the interstitium of the lamina propria. Based on the result of pathological tests and SEM, we considered that lanthanum had been taken up by histiocytes.
It is important to distinguish between the yellowish–white substance seen by the magnified NBI endoscopy and “white opaque substance” (WOS) [20, 21]. Yao et al. reported WOS obscures the microvessels that are just beneath the epithelium. However, in the present case, we could see microvessels on the yellowish–white substance, meaning that the yellowish–white substance exists beneath the sub-epithelial capillary network. Therefore, it can be concluded that magnified NBI endoscopy can be helpful in distinguishing between the uptake of lanthanum and WOS.
Our patient stopped taking lanthanum carbonate after its deposition was confirmed in the gastric mucosa. However, there have been no significant changes in the endoscopic findings, with the persistence of whitish granular mucosa in the gastric corpus and the depressed lesions surrounded by annular whitish mucosa in the antrum. As needed, we will continue to monitor his condition closely to observe any further changes.
In the present case, lanthanum deposition in the gastric mucosa was demonstrated by SEM–EDS. In SEM, an electron beam is directed at the sample, and electrons and X-rays discharged by the sample are detected to provide a three-dimensional picture of its surface structure. An energy-dispersive X-ray spectroscope is a device attached to a scanning electron microscope that detects characteristic X-rays and obtains information on the elements present in a given sample. “Characteristic X-rays” are multiple X-rays of varying energies characteristic of a particular element, and these are emitted when electrons from an electron beam collide with the atoms in a substance. Since each element emits a different pattern of characteristic X-rays, measuring the energy of the characteristics X-rays enables us to identify the elements present in the area irradiated by the electron beam. There are two methods used for EDS analysis: (1) spectral analysis to determine the elements deposited in the sample, (2) digital mapping for investigating the location of the deposited elements.
In our patient, histiocytes were identified by SEM, and digital mapping by EDS demonstrated the dense deposition of lanthanum phosphate in histiocytes. Lanthanum phosphate was also demonstrated in the interstitium, showing that this agent was not only taken up by histiocytes but also deposited in the interstitium. Previous studies have also demonstrated lanthanum phosphate deposition by SEM, but they did not show lanthanum phosphate deposition in the interstitium. Hence, our results provide evidence suggesting that free lanthanum phosphate in the interstitium is phagocytosed by histiocytes, offering an insight into the process of lanthanum phosphate deposition.
In summary, we reported that the case of lanthanum uptake by histiocytes in gastric mucosa has characteristic findings by magnified NBI endoscopy. We observed a yellowish–white substance within regular villous-like structures and enlarged regular vessels by magnified NBI endoscopy. Additionally, we proved that lanthanum together with phosphorus were densely distributed in histiocytes and sparsely in the interstitium by digital mapping via SEM–EDS.