(see Pulmonary Langerhans Cell Histiocytosis.)
Langerhans cell histiocytosis (LCH) is a proliferation of dendritic mononuclear cells with infiltration into organs locally or diffusely. Most cases occur in children. Manifestations may include lung infiltrates; bone lesions; rashes; and hepatic, hematopoietic, and endocrine dysfunction. Diagnosis is based on biopsy. Factors predicting a poor prognosis include age < 2 yr and dissemination, particularly involving the hematopoietic system, liver, lungs, or a combination. Treatments include supportive measures and chemotherapy or local treatment with surgery or radiation therapy as indicated by the extent of disease.
LCH is a dendritic cell disorder. It can cause distinct clinical syndromes that have been historically described as eosinophilic granuloma, Hand-Schüller-Christian disease, and Letterer-Siwe disease. Because these syndromes may be varied manifestations of the same underlying disorder and because most patients with LCH have manifestations of more than one of these syndromes, the designations of the separate syndromes (except for eosinophilic granuloma) are now mostly of historical significance. Estimates of the prevalence of LCH vary widely (eg, from about 1:50,000 to 1:200,000).
In LCH, abnormally proliferating dendritic cells infiltrate one or more organs. Bones, skin, teeth, gingival tissue, ears, endocrine organs, lungs, liver, spleen, lymph nodes, and bone marrow may be involved. Organs may be affected by infiltration, causing dysfunction, or by compression from adjacent enlarged structures. In about half of patients, more than one organ is involved.
Symptoms and Signs
Symptoms and signs vary considerably depending on which organs are infiltrated. Here, the syndromes are described by their historical designations, but few patients present with classic manifestations, and other than eosinophilic granuloma, these designations are no longer used.
Solitary or multifocal eosinophilic granuloma (60 to 80% of LCH cases) occurs predominantly in older children and young adults, usually by age 30; incidence peaks between ages 5 and 10 yr. Lesions most frequently involve bones, often with pain, the inability to bear weight, or both and with overlying tender (sometimes warm) swelling.
This syndrome (15 to 40% of LCH cases) occurs in children aged 2 to 5 yr and in some older children and adults. Classic findings in this systemic disorder include involvement of the flat bones of the skull, ribs, pelvis, scapula, or a combination. Long bones and lumbosacral vertebrae are less frequently involved; the wrists, hands, knees, feet, and cervical vertebrae are rarely involved. In classic cases, patients have proptosis caused by orbital tumor mass. Rarely, vision loss or strabismus is caused by optic nerve or orbital muscle involvement. Tooth loss caused by apical and gingival infiltration is common in older patients.
Chronic otitis media and otitis externa due to involvement of the mastoid and petrous portions of the temporal bone with partial obstruction of the auditory canal are fairly common. Diabetes insipidus, the last component of the classic triad that includes flat bone involvement and proptosis, affects 5 to 50% of patients, with higher percentages in children who have systemic disease and involvement of the orbit and skull. Up to 40% of children with systemic disease have short stature. Hyperprolactinemia and hypogonadism can result from hypothalamic infiltration.
This syndrome (10% of LCH cases), a systemic disorder, is the most severe form of LCH. Typically, a child < 2 yr presents with a scaly seborrheic, eczematoid, sometimes purpuric rash involving the scalp, ear canals, abdomen, and intertriginous areas of the neck and face. Denuded skin may facilitate microbial invasion, leading to sepsis. Frequently, there is ear drainage, lymphadenopathy, hepatosplenomegaly, and, in severe cases, hepatic dysfunction with hypoproteinemia and diminished synthesis of clotting factors. Anorexia, irritability, failure to thrive, and pulmonary manifestations (eg, cough, tachypnea, pneumothorax) may also occur. Significant anemia and sometimes neutropenia occur; thrombocytopenia is of grave prognostic significance. Parents frequently report precocious eruption of teeth, when in fact the gums are receding to expose immature dentition. Patients may appear abused or neglected.
LCH is suspected in patients (particularly young patients) with unexplained pulmonary infiltrates, bone lesions, or ocular or craniofacial abnormalities; and in children < 2 yr with typical rashes or severe, unexplained multiorgan disease.
X-rays are often done because of presenting symptoms. Bone lesions are usually sharply marginated, and round or oval, with a beveled edge giving the appearance of depth. However, some lesions are radiographically indistinguishable from Ewing sarcoma, osteogenic sarcoma, other benign and malignant conditions, or osteomyelitis.
Diagnosis is based on biopsy. Langerhans cells are usually prominent, except in older lesions. These cells are identified by a pathologist experienced in the diagnosis of LCH according to their immunohistochemical characteristics, which include cell surface CD 1a and S-100. Once diagnosis is established, the extent of disease must be determined by appropriate imaging and laboratory studies.
Prognosis is good for patients with both of the following:
With treatment, almost all such patients survive.
Morbidity and mortality are increased in patients with multiorgan involvement, particularly those with
With treatment, the overall survival rate for patients with multiorgan disease is about 80%. Death is more likely among at-risk patients who do not respond to initial therapy. Disease recurrence is common. A chronic remitting and exacerbating course may occur, particularly among adults.
Because these syndromes are rare and complex, patients are usually referred to institutions experienced in the treatment of LCH. The majority of patients should be treated using protocols developed by the Histiocyte Society (see the Histiocyte Society web site). General supportive care is essential and may include scrupulous hygiene to limit ear, cutaneous, and dental lesions. Debridement or resection of severely affected gingival tissue limits oral involvement. Seborrhea-like dermatitis of the scalp may diminish with use of a selenium-based shampoo twice/wk. If shampooing is ineffective, topical corticosteroids are used in small amounts and briefly in small areas.
Patients with systemic disease are monitored for potential chronic disabilities, such as cosmetic or functional orthopedic and cutaneous disorders and neurotoxicity as well as for psychologic problems that may require psychosocial support.
Many patients require hormone replacement for diabetes insipidus or other manifestations of hypopituitarism.
Chemotherapy is indicated for patients with multiorgan involvement. Protocols sponsored by the Histiocyte Society are used; treatment protocols vary according to the risk category. Almost all patients with a good response to therapy can stop treatment. Protocols for poor responders are under study.
Local surgery or radiation therapy is used for disease involving a single bone and, rarely, when multiple lesions or multiple bones are involved. Easily accessible lesions in noncritical locations undergo surgical curettage. Surgery should be avoided when it may result in significant cosmetic deformities, orthopedic deformities, or loss of function. Radiation therapy involving megavoltage equipment may be given to patients at risk of skeletal deformity, vision loss secondary to proptosis, pathologic fractures, vertebral collapse, and spinal cord injury or to patients with severe pain. Doses of radiation are considerably less than those used to treat cancer. Surgery and radiation therapy should be done by specialists experienced in treating LCH.
Patients with multiorgan disease that progresses despite standard therapy usually respond to more aggressive chemotherapy. Patients who do not respond to salvage chemotherapy may undergo bone marrow transplantation, experimental chemotherapy, or immunosuppressive or other immunomodulatory therapy.
Last full review/revision June 2013 by Jeffrey M. Lipton, MD, PhD
Content last modified November 2013