ArticleCureus2026
Recurrent Calciphylaxis With Discordant Parathyroid Hormone Trajectory in a Patient With HIV-Associated End-Stage Renal Disease: A Case Report.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Calciphylaxis, also termed calcific uremic arteriolopathy, is a rare and devastating complication of end-stage renal disease (ESRD). Its occurrence in patients with HIV-associated ESRD is sparsely characterized in the literature. We report a 36-year-old African American woman with ESRD secondary to longstanding hypertension and virologically suppressed HIV infection (CD4 count 348 cells/μL) who developed three discrete presentations of recurrent calciphylaxis over 18 months, with histopathologic confirmation at initial diagnosis and at first recurrence. At initial presentation (T1), intact parathyroid hormone (iPTH) was 806.5 pg/mL; she was treated with paricalcitol, sevelamer carbonate, and intravenous sodium thiosulfate (STS) but remained intermittently nonadherent to hemodialysis and prescribed therapies, with a single-pool Kt/V of 0.29 documented at recurrence. At second presentation 12 months later (T2), iPTH was 308.4 pg/mL despite active cutaneous lesions; management included surgical debridement, broad-spectrum antibiotics for superimposed polymicrobial soft tissue infection, continued STS, and dialysis intensification. Six months after T2 (T3), the patient represented with lesion expansion and new ulcerations, and iPTH had risen to 1,764.9 pg/mL alongside hypocalcemia and hyperphosphatemia, consistent with progression toward tertiary hyperparathyroidism. Parathyroidectomy was deferred at T2 and T3 because of acute infectious burden and uncontrolled hyperkalemia, respectively. This case illustrates the diagnostic and management complexity of recurrent calciphylaxis in HIV-associated ESRD, demonstrates how intermittent treatment adherence may produce highly discordant iPTH measurements that complicate threshold-based monitoring, and underscores the importance of multidisciplinary planning before surgical and metabolic barriers to parathyroidectomy accumulate.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.