What condition is most commonly associated with accessory spleens: idiopathic thrombocytopenic purpura (ITP), thrombotic thrombocytopenic purpura (TTP), schistosomiasis, or hereditary spherocytosis?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: November 2, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Accessory Spleens in Idiopathic Thrombocytopenic Purpura

The correct answer is (a) idiopathic thrombocytopenic purpura (ITP), as accessory spleens are clinically most relevant in this condition where they can cause treatment failure after splenectomy.

Clinical Significance in ITP

Accessory splenic tissue is found in up to 12% of splenectomized ITP patients, and assessment for accessory spleens should be considered in patients who relapse following an initial response to splenectomy 1. This represents the highest clinical relevance among the listed conditions because:

  • Approximately 20% of ITP patients who initially respond to splenectomy will relapse weeks, months, or years later 1
  • In patients who relapse after initial splenectomy response, the presence of accessory splenic tissue may explain the recurrence of thrombocytopenia 1
  • Imaging techniques can identify these accessory spleens, and almost all can be removed during surgery 1

Why ITP Over Other Conditions

Hereditary Spherocytosis Context

While accessory spleens are also clinically important in hereditary spherocytosis, the evidence shows:

  • Accessory spleens must be sought and removed at the time of splenectomy in hereditary spherocytosis patients 2
  • Recurrent hemolytic anemia can occur due to hypertrophied accessory spleens in hereditary spherocytosis 3
  • However, the question asks where accessory spleens are "most commonly found," and the ITP guidelines specifically quantify this at 12% of splenectomized patients 1

Other Conditions

  • Thrombotic thrombocytopenic purpura (TTP): Splenectomy is not a standard treatment for TTP, making accessory spleens clinically irrelevant in this condition 4
  • Schistosomiasis: No evidence provided links accessory spleens to this parasitic infection

Critical Clinical Pitfall

In patients who never responded to initial splenectomy, searching for accessory spleens is futile as response is extremely rare 1. This distinguishes between:

  • Relapsers after initial response → assess for accessory spleen
  • Non-responders from the start → accessory spleen unlikely to be the cause

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Thrombotic Thrombocytopenic Purpura (TTP) Clinical Manifestations and Diagnosis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.