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Although this may occur as the result of a rare primary syndrome in which an error of glyoxylate metabolism causes an overproduction of oxalate, it is more often seen as a secondary process characterized by increased enteric oxalate absorption. Here, we describe a patient with short bowel syndrome on long\u2010term parenteral nutrition support who developed a unique manifestation of systemic oxalosis, leading to deposition of oxalate crystals within the bone marrow contributing to pancytopenia. In this report, in addition to reviewing the literature on this presumably rare manifestation of oxalosis, we also discuss its pathogenesis in the setting of short bowel syndrome and its management, including prevention.<\/jats:p>","DOI":"10.1002\/jpen.2453","type":"journal-article","created":{"date-parts":[[2022,10,1]],"date-time":"2022-10-01T07:59:15Z","timestamp":1664611155000},"page":"165-170","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Bone marrow oxalosis with pancytopenia in a patient with short bowel syndrome: Report of a case and review of the literature"],"prefix":"10.1002","volume":"47","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6161-7088","authenticated-orcid":false,"given":"Jamie L.","family":"Bering","sequence":"first","affiliation":[{"name":"Division of Gastroenterology and Hepatology Mayo Clinic Arizona Scottsdale Arizona 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