ArticleJCEM case reports2026
Delayed Diagnosis of McCune-Albright Syndrome in Adulthood Revealed by Spinal Fibrous Dysplasia: Report of 2 Cases.
Article in JCEM case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- Multidisciplinary approach and clinical management of McCune-Albright syndrome.Frontiers in endocrinology · 2026Review
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Authors and funding
6 authors.
Funding
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Abstract
McCune-Albright syndrome (MAS) is a rare genetic disorder characterized by fibrous dysplasia of bone, café-au-lait skin pigmentation, and endocrine abnormalities. Adult presentation with spinal fibrous dysplasia, although previously reported, is uncommon and diagnostically challenging. We report 2 cases of MAS diagnosed in young women who initially presented with persistent back pain. Both patients underwent imaging studies that revealed multiple lytic lesions in the spine, raising concern for metastatic disease. Further evaluation confirmed the presence of polyostotic fibrous dysplasia without evidence of malignancy. Both patients had a history of precocious puberty, consistent with the syndrome's known manifestations. In 1 case, the diagnosis was supported by detection of a somatic
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