ArticleCureus2026
A Rare Case of Cutaneous Lymphomatoid Granulomatosis: A Case Report and Literature Review.
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
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Lymphomatoid granulomatosis is a rare lymphoproliferative disease caused by dysfunction of host surveillance of Epstein-Barr virus (EBV)-infected B cells, which predominantly affects male adults, with a median onset at 46 years. Diagnosis can be challenging due to its nonspecific symptoms and the need for careful histopathological evaluation, particularly in atypical presentations. Here, we present a case of a 42-year-old Black man from Senegal with no past medical history who presented with a chronic, non-healing ulcer on his right upper extremity that had worsened over six months. Family history revealed a sister with kidney disease who required early dialysis. Initial vital signs showed a blood pressure of 178/123 mmHg and a heart rate of 127 beats/min, with normal temperature and oxygen saturation. A 4 × 5 cm crusted, non-tender stage 3 ulcer with hyperpigmented edges was found on his right arm. Laboratory tests showed pancytopenia, stage 5 chronic kidney disease with nephrotic-range proteinuria, and normocytic anemia. Blood cultures, HIV, and leishmaniasis tests were negative, and chest radiograph findings were normal. Initial evaluation also revealed chronic hepatitis B infection. CT raised concern for osteomyelitis, but MRI was negative. Skin biopsy showed nonspecific inflammatory changes, and cultures revealed methicillin-sensitive
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.