Letterer–Siwe disease

Letterer–Siwe disease
Other names: Acute and disseminated Langerhans cell histiocytosis
This condition is inherited in an autosomal recessive manner

Letterer–Siwe disease, also known as multi system variant histiocytosis, is a type of Langerhans cell histiocytosis (LCH), that may affect several organs, typically in young children.^[1]

It causes approximately 10% of LCH disease and is the most severe form.^[2] Prevalence is estimated at 1:500,000 and the disease almost exclusively occurs in children less than three years old.^[3] The name is derived from the names of Erich Letterer and Sture Siwe.

Signs and symptoms

Letterer-Siwe is characterized by skin lesions, ear drainage, large lymph nodes, osteolytic lesions, and large liver and spleen.^[4] The skin lesions are scaly and may involve the scalp, ear canals, and abdomen.^[4]

Cause

Oncogenic mutation of BRAF 50-70% cases

Diagnosis

The diagnosis was established by histopathology and electron microscopy.--2.  In Abt-Letterer-Siwe disease, the racket-like Langerhans cell granules are found by electron microscopy within the specific infiltrating cells. The demonstration of these organelles allows the unequivocal diagnosis in cases with uncharacteristic clinical or histopathological appearance. The same structures are characteristic of Hand-Schüller-Christian disease and of eosinophilic granuloma. The electron microscopic findings confirm the grouping of these three diseases together as "histiocytosis X".

Prognosis

The disease is often rapidly fatal, with a five-year survival rate of 50%. The development of thrombocytopenia is a poor prognostic sign.^[2]

References

External links