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juvenile xanthogranuloma

Description

What is Juvenile Xanthogranuloma?

Juvenile xanthogranuloma (JXG) is a rare benign histiocytic proliferation that develops in infants and young children [5]. It is a type of non-Langerhans cell histiocytosis, which means it does not involve the Langerhans cells, a type of immune cell found in the skin [4].

Clinical Presentation

The clinical presentation of JXG is characterized by single or multiple yellow and brown skin nodules, most often found on the face and neck [3]. These nodules are usually harmless and have no effect on the overall health of the person affected [6]. They can also be found on the scalp, upper body, and other areas.

Characteristics

JXG is a benign and typically self-limited skin disorder that is not commonly associated with systemic manifestations [7]. It is a lump in the skin that is usually harmless and has no effect on the overall health of the person affected. JXG is also known to be a self-healing condition, meaning it will resolve on its own without any treatment.

Types

JXG can occur as solitary or multiple lesions, and can range from small papules to larger nodules [8]. It is the most common type of non-Langerhans cell histiocytosis, characterized by the occurrence of one or more reddish or yellowish skin lesions [9].

Overall, juvenile xanthogranuloma is a rare but benign condition that affects young children and infants. While it can be alarming to see these skin nodules, they are usually harmless and will resolve on their own without any treatment.

References: [3] - The clinical presentation of this disease is characterized by single or, rarely, multiple yellow and brown skin nodules, most often found on the face and neck. [4] - May 5, 2023 — INTRODUCTION. Juvenile xanthogranuloma (JXG) is a benign, proliferative disorder belonging to the broad group of non-Langerhans cell ... [5] - Aug 27, 2024 — Juvenile xanthogranuloma (JXG) is a rare benign histiocytic proliferation that develops in infants and young children. [6] - JXG is a lump in the skin, often on the scalp, face, neck or upper body. It is usually harmless and has no effect on the overall health of the person affected. [7] - Juvenile xanthogranuloma (JXG) is a benign and typically self-limited skin disorder that is not commonly associated with systemic manifestations. [8] - Aug 27, 2024 — Juvenile xanthogranuloma (JXG) is a rare benign histiocytic proliferation that develops in infants and young children. [9] - May 5, 2023 — INTRODUCTION. Juvenile xanthogranuloma (JXG) is a benign, proliferative disorder belonging to the broad group of non-Langerhans cell ...

Additional Characteristics

  • A rare benign histiocytic proliferation that develops in infants and young children.
  • A type of non-Langerhans cell histiocytosis.
  • Single or multiple yellow and brown skin nodules, most often found on the face and neck.
  • A lump in the skin that is usually harmless and has no effect on overall health.
  • A self-limited skin disorder that is not commonly associated with systemic manifestations.
  • Can occur as solitary or multiple lesions, ranging from small papules to larger nodules.
  • The most common type of non-Langerhans cell histiocytosis.

Signs and Symptoms

Common Signs and Symptoms of Juvenile Xanthogranuloma

Juvenile xanthogranuloma (JXG) is a rare skin condition that primarily affects young children. While most individuals with JXG are asymptomatic, some common signs and symptoms include:

  • Skin lesions: The skin lesions of JXG usually present as reddened, yellowish-tan, slightly raised bumps [5][7].
  • Location: These lesions generally appear on the head, neck, and trunk, although they can occur elsewhere on the body [5][7].
  • Size and shape: The lesions are typically small to medium in size and may be solitary or multiple.
  • Color: They have a reddened or yellowish-tan color.

In some cases, JXG can be associated with systemic manifestations, which may include:

  • Anemia
  • Thrombocytopenia (low platelet count)
  • Leukocytosis (high white blood cell count)
  • Lymphadenopathy (enlarged lymph nodes)
  • Hepatosplenomegaly (enlarged liver and spleen)

These systemic symptoms are relatively rare and usually occur in more severe cases of JXG.

References:

[5] The skin lesions of JXG usually present as reddened, yellowish-tan, slightly raised bumps. They generally appear on the head, neck, and trunk although they can ... [7] The skin lesions of JXG usually present as reddened, yellowish-tan, slightly raised bumps. They generally appear on the head, neck, and trunk although they can ...

Additional Symptoms

  • Lymphadenopathy (enlarged lymph nodes)
  • Thrombocytopenia (low platelet count)
  • Skin lesions
  • Hepatosplenomegaly (enlarged liver and spleen)
  • Leukocytosis (high white blood cell count)
  • anemia

Diagnostic Tests

Treatment

Differential Diagnosis

Additional Information

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A non-Langerhans-cell histiocytosis is characterized as a benign skin lump or bump caused by a collection of cells called histiocytes. These may be red, orange or tan at first, but over time may become more yellow in color. These bumps usually appear on the head, neck and trunk.
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