Fischer-Bruges Syndrome

Fischer-Bruges syndrome: picture of the disease

**Fisher–Bruges syndrome** is a syndrome characterized by hypopigmentation of depigmented areas of the face and skin of varying frequency in the form of whitish areas of a scabrous appearance, symmetrically located on the posterolateral surface of the head of the left ossicular bone, the molecule, the upper flaps of the masticatory muscles of the face, the bottom of the upper segment of the orbit, the upper surface of the superior processes of the chin lying to the muscles, the dorsal surfaces of the tips of the lip, the lateral wall of the vestibule of the mouth, a hypopigmented area in the form of a pale “areolar glow” around the preorbital vein, the femur above the superior labial groove, the paciform (labial) iliac protrusions, the medial side of the eyebrows and ciliary edge, zygomatic region, combined with hypodermia, atrophy of subcutaneous fatty tissue, the appearance of small senile wrinkles, impaired pigmentation of the perineal area, as well as swelling of the pubic symphysis.

The most common way of manifestation of the Fischer-Brugge symptom complex is “Egg”, which is a skin defect with foci of whitish depigmentation, of varying degrees of severity, spreading both from the center to the sides and from border to border. This anomaly for women is often the cause

Fischer-Brugman syndrome is a rare disease characterized by inflammation of the subcutaneous fatty tissue in the cheek area. The disease manifests itself in the form of redness, swelling, and sometimes itching of the skin, which can be permanent or temporary. There are several forms of this disease, including acute, chronic, impetigo, hyperplastic and annular.

Fischer-Brugmann syndrome is caused by various bacterial or fungal infections, such as staphylococci, streptococci or yeast. Risk factors for developing the disease include clogged skin pores, allergies, Parkinson's disease, obesity and high blood sugar.