# From Common Symptom to Critical Diagnosis: Vertigo as a Clue to Thrombotic Thrombocytopenic Purpura

**Authors:** Aysche J Stern, Nicholas R Munoz, Reda Khan, Chibuike C Agwuegbo, Salma Yasin, Marie Pearson, Fatima Gauhar

PMC · DOI: 10.7759/cureus.78305 · Cureus · 2025-01-31

## TL;DR

A rare blood disorder was misdiagnosed as a common inner ear issue, highlighting the need to consider TTP in patients with unusual symptoms and lab results.

## Contribution

This case highlights the importance of recognizing TTP in patients with atypical presentations and non-specific symptoms.

## Key findings

- The patient initially presented with vertigo and normal hemoglobin but later developed hemolytic anemia and severe thrombocytopenia.
- She was eventually diagnosed with TTP and treated with plasma exchange and rituximab.
- The case underscores the need for early suspicion of TTP despite initial atypical symptoms.

## Abstract

Thrombotic thrombocytopenic purpura is a hematologic disease with a high mortality rate that affects multiple organ systems. It is caused by a deficiency of a metalloprotease known as the ADAMTS-13 enzyme. Patients can present with fever, hemolytic anemia, thrombocytopenia, kidney injury, and neurological symptoms. Here we present a case of a female with TTP who was initially diagnosed with benign paroxysmal positional vertigo (BPPV). Her initial symptoms were vertigo, blurry vision, and gait imbalance, which were accompanied by elevated total bilirubin, acute kidney injury, thrombocytopenia, and normal hemoglobin. When the patient followed up in her primary care clinic, she was found to have worsening renal function, hemolytic anemia, and severe thrombocytopenia. She was subsequently diagnosed with TTP and referred to the emergency department (ED) where she received emergent treatment with therapeutic plasma exchange (TPE) and later rituximab. This case stresses the importance of considering TTP in patients presenting with symptoms and laboratory values suggestive of the disease, even when anemia is not present.

## Linked entities

- **Proteins:** ADAMTS13 (ADAM metallopeptidase with thrombospondin type 1 motif 13)
- **Diseases:** Thrombotic thrombocytopenic purpura (MONDO:0018896), benign paroxysmal positional vertigo (MONDO:8000018), hemolytic anemia (MONDO:0003664), acute kidney injury (MONDO:0002492)

## Full-text entities

- **Genes:** ADAMTS13 (ADAM metallopeptidase with thrombospondin type 1 motif 13) [NCBI Gene 11093] {aka ADAM-TS13, ADAMTS-13, C9orf8, VWFCP, vWF-CP}
- **Diseases:** hematologic disease (MESH:D006402), TTP (MESH:D011697), thrombocytopenia (MESH:D013921), BPPV (MESH:D065635), blurry vision (MESH:D014786), hemolytic anemia (MESH:D000743), Vertigo (MESH:D014717), acute kidney injury (MESH:D058186), neurological symptoms (MESH:D009461), anemia (MESH:D000740), gait imbalance (MESH:D020234), kidney injury (MESH:D007674), fever (MESH:D005334)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11872677/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11872677/full.md

## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC11872677/full.md

---
Source: https://tomesphere.com/paper/PMC11872677