目录
In the diagnosis of oral and maxillofacial diseases, clinicians use specific terms to describe unique physical findings and reactions. Many of these are eponymous signs—named after the physicians who discovered them—that help identify conditions ranging from Pemphigus to Systemic Sclerosis. There are two tables adapted from Clinical Guide to Oral Diseases listing common clinical signs and phenomena, their definitions, and the oral or systemic diseases associated with them.
Table 1: Clinical Signs
| Name | Clinical findings | Diseases |
|---|---|---|
| Asboe-Hansen sign | Blister spreading with pressure | Pemphigus, bullous pemphigoid |
| Auspitz sign | Pin-point bleeding after removal of scales | Psoriasis |
| Barnett’s sign | Ridging and tightening of neck | Scleroderma |
| Buttonhole sign | Invagination of neurofibromas with pressure | Neurofibromatosis-NF1 |
| Crowe’s sign | Axillary freckles | Neurofibromatosis-NF1 |
| Forchheimer’s sign | Petechiae or enanthema on soft palate | Infectious mononucleosis; rubella |
| Gorlin’s sign | Tongue touching the nose | Ehlers-Danlos syndrome |
| Meffert’s sign | Ectopic sebaceous glands on lips causing a lipstick-like mark left on the rim of a glass mug after consuming a hot beverage | Fordyce disease |
| Nikolsky’s sign | Peeling and new bullae formation with rubbing off the unaffected skin or oral mucosa | Pemphigus |
| Reverse Nikolsky’s sign | Pseudoepithelial peeling | Toxic epidermal necrolysis; staphylococcal scaled skin |
| Osler’s sign | Blue-black sclera | Alkaptonuria |
| Stafne’s sign | Widening of the periodontal ligament space | Systemic sclerosis |
Table 2: Clinical Phenomena
| Name | Clinical findings | Diseases |
|---|---|---|
| Bell’s phenomenon | Inability to close the affected eye | Facial nerve palsy |
| Brocq’s phenomenon | Subepidermal hemorrhage, which occurs on careful scraping of a classical lesion of skin disease | Lichen planus |
| Isotopic phenomenon | Occurrence of a different or unrelated dermatological disease at the site of the healed disease (commonly herpes zoster) | Herpes zoster |
| Kasabach-Merrit phenomenon | Triad of vascular tumors, thrombocytopenia, and bleeding diathesis. | Infantile hemangiomas, Blue rubber bleb nevus |
| Koebner phenomenon | Development a new similar lesions along lines of trauma | Psoriasis, lichen planus, vitiligo |
| Koebner inverse phenomenon | A skin condition which inhibits the development of another autoimmune disease | Psoriasis and alopecia areata |
| Koebner remote reverse phenomenon | Spontaneous repigmentation is seen in distant patches after autologous skin graft surgery | Vitiligo |
| Koebner reverse phenomenon | Clearance of an area of skin disease after trauma | Psoriasis |
| Pathergy phenomenon | An erythematous papule of more than 2 mm at the site of a non-specific trauma like pricking with a 20–22-gauge needle | Behcet’s disease, Sweet’s syndrome |
| Raynaud’s phenomenon | Episodic changes in blood flow in the cutaneous vasculature in cold weather | Connective tissue diseases, Sjogren’s syndrome |
| Rebound phenomenon | Reappearance of a skin disease after stopping steroid treatment | Various dermatosis |
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