Benign lymphoepithelial lesion

Benign lymphoepithelial lesion
Other names	Mikulicz' disease
Specialty	Gastroenterology

Benign lymphoepithelial lesion or Mikulicz' disease is a type of

Presentation

Benign lymphoepithelial lesion is most likely to occur in adults around 50 years of age. Approximately 60–80% of those affected are female. The gland affected has a diffuse swelling. The swelling can be asymptomatic, but mild pain can also be associated. This condition occurs often in those with HIV infection.^{[citation needed]}

Most cases of benign lymphoepithelial lesions appear in conjunction with Sjögren's syndrome. When Sjögren's syndrome is present, the swelling is usually

In 80% of cases, the parotid gland is affected. Lacrimal glands are also affected.^[citation needed]

Histology

There is a marked lymphoplasmacytic infiltration. Lymphoid follicles surround solid epithelial nests, giving rise to the 'epimyoepithelial islands', that are mainly composed of ductal cells with occasional myoepithelial cells. Excess hyaline basement membrane material is deposited between cells, and there is also acinar atrophy and destruction.^{[citation needed]}

Treatment

Treatment usually consists of observation unless the patient has concern, there is pain, drainage, or other symptoms related to the lesion. Surgical removal of the affected gland would be recommended in those cases. Another treatment option would be aspiration, which can be repeated multiple times. This is commonly performed in those who are debilitated or in those whose benefit from surgery would be outweighed by the risks. Prognosis is usually good; rarely this condition may devolve into lymphoma, or could actually represent 'occult' lymphoma from the outset.^{[citation needed]}

Eponym

Historically, bilateral parotid and lacrimal gland enlargement was characterized by the term Mikulicz's disease if the enlargement appeared apart from other diseases. If it was secondary to another disease, such as tuberculosis, sarcoidosis, lymphoma, and Sjögren's syndrome, the term used was Mikulicz's syndrome. Both names derive from Jan Mikulicz-Radecki, the Polish surgeon best known for describing these conditions.^[1][2]

In more recent times, the terms "Mikulicz's disease" and "Mikulicz's syndrome" were viewed as ambiguous and outdated by some sources.^[3]

Today Mikulicz's disease is considered to be a subtype of IgG4-related disease, usually accompanied by involvement of one or more other organs in the body.^[4]

See also

• Lymphoepithelial lesion

References