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Living with Reticulohistiocytic granuloma

A rare, non-cancerous skin or soft tissue lump, usually yellow to reddish-brown, most often seen on the trunk or limbs.

Understanding Reticulohistiocytic granuloma

Reticulohistiocytic granuloma is a rare, non-cancerous (benign) lump in the soft tissue caused by a buildup of immune cells.

It is also called reticulohistiocytoma. It belongs to a group of conditions called histiocytosis, where immune cells called histiocytes multiply quickly in the skin or soft tissue. The lump is smooth and firm and appears on the trunk or limbs. It has historically been found in young adults, a little more often in males.

Signs & symptoms

GARD doesn't list specific symptoms for this condition yet. Its summary describes a lump:

  • Firm, smooth lump or nodule
  • Yellow to reddish-brown color
  • Usually on the trunk or limbs

Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.

Diagnosis

  1. Talk with your doctor

    Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.

  2. See a specialist

    Your doctor may refer you to a specialist who knows rare conditions.

  3. Ask which tests can help

    Your care team will decide which exams and tests can confirm the diagnosis.

  4. Connect with expert centers

    Histiocytosis Association may keep lists of experts for this condition.

Care & treatment

Care team
A doctor familiar with rare conditions, plus specialists as needed
Expert care
Expert lists: Histiocytosis Association
Treatment
GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
Research
Clinical trials and observational studies may be options. See the research section below.

General information, not medical advice. Your care team makes the decisions.

Everyday life

Living with a rare condition is easier with support.

  • Connect with Histiocytosis Association
  • Keep notes on symptoms, changes and questions for appointments
  • Ask about patient registries that help research
  • Look into financial aid and travel resources for care visits
Bring these questions to your next doctor visit
How is this lump told apart from other skin lumps?
Does it need to be removed or watched over time?
Which specialist should follow this condition?

Quick facts

GARD says the trigger that makes the immune system react is not well understood. GARD does not list a gene or inheritance pattern.

Also known as: giant cell histiocytoma; reticulohistiocytic granuloma (morphologic abnormality); reticulohistiocytoma; reticulohistiocytoma cutis; solitary reticulohistiocytoma

Patient organizations

Source: NIH GARD · Reticulohistiocytic granulomaGARD ID 12967 · GARD page updated September 2026 · Plain-language summary by Know Rare; editorial review pending. General information, not medical advice.

You are more than your diagnosis

Perspectives from people navigating life with Reticulohistiocytic granuloma.

Explore the Reticulohistiocytic granuloma blog

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Explore actively recruiting Reticulohistiocytic granuloma studies with HealthSpark.

HealthSpark

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  • Recruiting studies from ClinicalTrials.gov
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  • Eligibility is confirmed by the study team

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Powered by HealthSpark, our AI chat helper · Study information from ClinicalTrials.gov · Eligibility is confirmed by the study team.

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