Oral and Skin Lesions: Clinical Features and Pathology

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Oral and Dermatological Lesions: Clinical Insights

Oral Candidiasis

  • Pseudomembranous Candidiasis (Thrush): Characterized by white, "skim milk" like pseudomembranes.
  • Erythematous Oral Candidiasis: Presents as red, erythematous areas, often a sequel to thrush.
  • Chronic Hyperplastic Candidiasis: Appears as persistent white plaques, commonly seen in older patients with acrylic prostheses.
  • Chronic Atrophic Oral Candidiasis: Associated with acrylic prostheses (e.g., upper suction chamber dentures), presenting as red, atrophic mucosa.

Mucocutaneous Inflammatory Conditions

  • Lichen Planus:
    • Can present as reticular (thorny/lace-like), papular, or erosive lesions.
    • Potentially premalignant, especially the erosive form.
    • Clinical presentation includes white or violet lesions on the buccal mucosa and gingiva.
  • Psoriasis (Skin Lesions):
    • Characterized by pink-salmon plaques covered with silvery scales.
    • Removal of scales reveals bleeding points (Auspitz sign).
    • Stress can exacerbate symptoms.

Benign Tumors and Proliferations

  • Keratoacanthoma:
    • Rapidly growing tumor originating from hair follicles or sebaceous glands.
    • Abrupt onset, often spontaneously regresses.
    • Presents as a nodule with a central keratin plug or crater.
  • Condyloma Acuminatum (Genital Warts):
    • Caused by Human Papillomavirus (HPV).
    • Can manifest as oral lesions, potentially transmitted via saliva.
    • Often presents as multiple, verrucous lesions.
  • Verruca Vulgaris (Common Wart):
    • Typically presents as 1-3 nodules.
    • Can occur on the ventral surface of the tongue or lips.
  • Pyogenic Granuloma:
    • Chronic Pyogenic Granuloma: Inflamed gingiva, tongue mucosa, and buccal mucosa, appearing as red, bleeding, or yellowish nodular areas.
    • Pyogenic Granuloma of Pregnancy (Pregnancy Tumor): Hormonally induced, localized lesion, often associated with generalized gingivitis during pregnancy.
    • Parulis (Gum Boil) related Pyogenic Granuloma: An inflammatory lesion originating from pus discharge via a chronic dentoalveolar abscess fistula, often associated with a localized tooth abscess.
  • Pulp Polyp (Hyperplastic Pulpitis):
    • Common in molars of young children.
    • Proliferates, forming granular pulp tissue.
    • Usually asymptomatic.
    • Treatment often involves extraction or endodontic therapy.
  • Irritation Fibroma (Pseudo-Fibroma):
    • Often caused by chronic irritation (e.g., biting).
    • Presents as an ulcerated, keratotic, or nodular area, commonly on the inner cheek.
    • Differential diagnosis includes a true fibroma.
  • Traumatic Neuroma (Amputation Neuroma):
    • A soft, often painful nodule.
    • Results from the proliferation of Schwann cells attempting to regenerate a severed nerve, but unable to form a functional connection.
  • Peripheral Giant Cell Granuloma (Reactive Lesion):
    • Often occurs at extraction sites, especially where a bone spicule remains.
    • Can be associated with ill-fitting prostheses.
    • Typically red-wine in color.
  • True Fibroma:
    • Normal color, often keratinized.
    • Slow-growing.
    • Differential diagnosis includes irritation fibroma, which is often red and inflamed.
  • Giant Cell Fibroma:
    • Can occur on any oral mucosa, frequently on the anterior third of the tongue.
    • Asymptomatic with a long evolution.
  • General Fibroma Characteristics:
    • Some fibrous lesions can be long-standing, firm, and immobile.
    • May be found on the maxillary skin.
  • Peripheral Ossifying Fibroma:
    • Originates from periosteum or periodontal ligament cells.
    • Affects adults and young children.
    • Histologically, it may contain bone (ossifying) or cementum (cementifying) within a fibrous capsule.
    • Immature forms are termed 'immature ossifying fibroma' or 'immature cementifying fibroma'.

Nerve Sheath Tumors

  • Neurilemoma (Schwannoma):
    • Benign neoplasm of Schwann cells.
    • Commonly found on the tongue.
    • Firm, hard, movable, and typically white or pink.
    • Histologically characterized by Antoni A (palisading Schwann cells forming Verocay bodies) and Antoni B areas.
  • Multiple Neurilemomas/Schwannomas:
    • Often associated with Neurofibromatosis Type 1 (Von Recklinghausen's disease).
    • More common in men.

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