Supplementary Material for: The Rare Trio: Concomitant Bone Marrow Involvement by Smolderi

A detailed medical case report documents a 67-year-old male patient with three concurrent rare disorders. The text includes diagnostic workup details, 24 months of follow-up data, and a literature review. The author is listed as 'figshare admin karger' and the material was last updated on April 16, 2026.

Use Cases

• Literature review and case comparison based on the documented review of fewer than 15 published cases of SM with plasma cell dyscrasias.
• Analysis of diagnostic pathways based on the described use of mass spectrometry for amyloid typing and KIT D816V mutation testing.
• Study of clinical management strategies based on the documented 24-month active surveillance follow-up period.

Strengths

• Includes a detailed 24-month patient follow-up period.
• Provides proteomic confirmation of amyloid subtype via mass spectrometry.
• Released under a permissive CC-BY-4.0 license for reuse.

Limitations

• The dataset is a single case report (19.2 KB), representing a very limited scope.
• Column-level documentation is absent; field semantics must be inferred after download.
• Row count is unknown, which may limit suitability assessment.

Provenance

Source

figshare

Collection Method

Likely contains a single authored medical case report and literature review.

Time Range

The case includes approximately 24 months of documented patient follow-up.

Freshness

Last updated 2026-04-16 07:55:15; freshness should be verified.

Geography

Patient is of Egyptian descent; specific location is not detailed.