Mucinoses, Lichen Planus and Related Conditions KCOM/Texas Consortium NE Regional Medical Center What is Mucin? • Fibrillar matrix in dermis called ground substance, created by.
Download ReportTranscript Mucinoses, Lichen Planus and Related Conditions KCOM/Texas Consortium NE Regional Medical Center What is Mucin? • Fibrillar matrix in dermis called ground substance, created by.
Mucinoses, Lichen Planus and Related Conditions KCOM/Texas Consortium NE Regional Medical Center What is Mucin? • Fibrillar matrix in dermis called ground substance, created by fibroblasts. • GS= acid mucopolysaccharides that bind 1000 times their own volume in water • Adding sulfates to the AMPs creates Chondroitin Sulfate and Heparin, the 2 primary dermal mucins H&E: GA: Wispy bluish, feathery material between collagen bundles Colloidal Iron Staining: GA Mucin – wispy, feathery Mucin Stains • • • • Colloidal Iron Alcian Blue Toluidine Blue Incubation of tissue in hyaluronidase eliminates the staining, confirming the presence of mucin Excess Mucin found in….. • Epithelial – MF, VV, Spongiotic Dermatitis, BCC, SCC, KA. • Dermal – Epithelial, Mesenchymal, Neural tumors, SLE, DM, Scleroderma, Degos, s/p UV/PUVA, GA, GVHD. • Follicular – Myeloproliferative CAs, Spongiotic, SLE, HT LP, Bites, Angiolymphoid hyperplasia with eosinophilia, Lichen striatus, Sarcoid, Photodermatitis, Familial reticuloendotheliosis Lichen Myxedematosus Lichen Myxedematosus • • • • Aka Papular Mucinosis Generalized = Scleromyxedema Onset age 30-80 Multiple waxy 2-4mm dome shaped or flat topped papules, usu. linear array • Acral: dorsal hands, face, elbows, and extensor extremities • Histopathology of lichen myxedematosus (discrete type). Mucin deposits splay collagen bundles in the dermis, but there is only slight fibroblast proliferation and no sclerosis. • Lichen myxedematosus of the discrete type demonstrating mucin accumulation in the dermis. Alcian blue stain (pH 2.5). Scleromyxedema • Woody, fibrous sclerosis of skin • Lesions coalesce to form leonine facies • Decreased ROM of hands, lips and extremities • GI: Dysphagia is • most common symptom Scleromyxedema: Systemic • Pulmonary • Proximal Muscle weakness • Carpal Tunnel Synd. • Peripheral Neurop. • Raynauds • IgG lambda paraproteinemia • Myeloma Increased fibroblasts and mucin in the reticular dermis Scleromyxedema. Typical triad of fibrosis, proliferation of irregularly arranged fibroblasts and interstitial deposits of mucin in the upper and midreticular dermis. Scleromyxedema • • • • • • Shares many features with scleroderma. Oral retinoids Immunosuppressives Extracorporeal photochemotherapy Melaphan Overall prognosis is poor. Papular Mucinosis and AIDS • • • • Widespread Not associated with a paraprotein Always seen in advanced HIV disease If assoc. with eczematoid dermatitis, clears when eczema clears • Oral retinoids Acral Persistent Papular Mucinosis • Usually women • Few to 100 bilaterally symmetrical 2 to 5mm, flesh colored papules • Always on hands and wrists. • Rarely elbows and knees • No paraprotein, no systemic dz • H&E: Increased mucin, but not fibroblasts Acral Persistent Papular Mucinosis Scleredema • Stiffening and hardening of the subcutaneous tissues as if they were infiltrated with paraffin. • With DM II (men); without DM II (women) • Begins on the neck, may spread symmetrically to arms, shoulders and back • Skin waxy, wood-like. • Demarcation poor if no DM, good if DM Scleredema without DM II • • • • • • • • F>M 2:1, Poorly demarcated edges 25% Streptococcal infection Paraproteinemia usually IgG, Myeloma Cardiac arrhythmias. Upper GI dysphagia, tongue involvement Pleural, pericardial or peritoneal effusion If infection precedes it, 50% resolve 2-3 yrs. Therapy is of no value, except 2 cases Cyclosporine was reported as beneficial. Scleredema with DM II • • • • • • • Most common, well demarcated edges M>F 10:1, usually obese Sharp step off at lesion edge Persistent erythema & folliculitis possible Controlling DM II has no effect on skin No visceral disease or paraprotein Therapy is useless, but case reports show benefit with IV PCN, PUVA, Electron Beam Scleredema Clinical Photo REM Syndrome • • • • • • • • Reticular Erythematous Mucinosis Aka Plaque-like Cutaneous Mucinosis Women, 3rd -4th decades of life Frequently follows intense sun exposure, and often pregnancy, OCPs, menses DIF, ANA negative MC midline chest & back Reticulate or plaque-like appearance Antimalarials often helpful REM SYNDROME Cutaneous Focal Mucinosis • Solitary lesions that resemble neurofibromas, cyst, BCC • Face, neck, trunk, extremities • Adulthood • Tx: Surgical excision Self-healing Juvenile Cutaneous Mucinosis • Sudden onset, age 5 to 15 • Skin lesions and polyarthritis x a few mos. • Ivory white papules head, neck, trunk and periarticular • Hard edema of periorbital area/face • TSH, IgG normal • H&E dermal mucin • Prognosis excellent Cutaneous Mucinosis of Infancy • 3 cases, onset birth-3 months of age • 2-8mm papules trunk, extremities, especially backs of hands • TSH, Paraprotein negative • Existing lesions remain, new lesions gradually accumulate • H&E: papillary dermal mucin, no fibroblasts Follicular Mucinosis • Aka Alopecia Mucinosa, 3 groups • MC young, head, neck arms, resolves in 2 mos to 2 years • 2nd group, larger more numerous lesions, takes several years to resolve • 3rd group, older, CTLC • 30% of FM patients have MF • Any patient >30 yo with FM, look for MF Follicular papules merging into a scaly plaque with alopecia MF associated follicular mucinosis H&E: asterisks mark large collections of mucin within cells of the sebaceous gland and outer root sheath with mixed dermal infiltrate • Treatments for Follicular Mucinosis after you have ruled out MF: • • • • • • Topical or oral corticosteroids Dapsone PUVA, Radiation therapy Interferon alfa-2b Mepacrine Indomethacin Myxoid Cysts • MC terminal dorsal or lateral fingers • Solitary 5-7mm opalescent or skin colored asymptomatic swellings of the PNF or DIP • NO CYSTIC LINING, not a true cyst • Synovial origin still debated • TX: I&D, Cryo, IL steroids, Fulguration of the base after draining. Meticulous excision including “stalk” by Salasche in 11 pts, no recur. •Groove of nail plate secondary to lesional pressure to the nail matrix Case of dermatomyositis presenting with cutaneous mucinosis as the sole manifestation. A malignancy screen revealed an underlying nasopharyngeal carcinoma. (J Am Acad Dermatol 2003;48:S41-2.) Lichen Planus • A disease of the skin, hair follicles and mucous membranes. • Mnemonic the 5 P’s • Wickham’s Striae, flat topped papules • Pruritis is paroxysmal, rubbing > scraching • Flexor wrists, trunk, medial thighs, shins, dorsal hands, glans penis Plentiful Purple Pruritic Polygonal Papules Wickham’s striae: gray or white puncta or streaks that cross the lesion 5-10% of LP cases have nail changes including pterygium, longitudinal grooving, onycholysis, splitting and peculiar midline fissure. • • • • • • Oral LP Ulcerative Reticulate Atrophic Risk of SCC 1/200 cutaneous LP pts develop oral SCC • 1/100 oral LP pts develop SCC over 3 year period • Mouth, anus are risk areas too. A - Annular LP – most commonly found on lips or penis. Central hyperpigmentation is characteristic Bullous LP Usually shins, as individual lesions merge, they vesiculate centrally. Often resolves spontaneously Lichen Planus Pemphigoides • Rare • Typical LP patients who experience bullae on top of their LP plaques • DIF positive for 180kd BPAg2 antigen • Treat like Bullous Pemphigoid Hypertrophic LP Linear LP – Aka Zosteriform 1% of LP cases Blaschko’s lines, not dermatomal Hepatitis C • Rate in LP pts between 4% and 38% • Japan: Hep C = 8%, LP w/ HepC = 60% • LP patients with Hep C are more likely to have erosive mucous membrane dz. • TX of Hep C w/ Alpha INF may induce LP. • Primary biliary cirrhosis & LP may coexist; ↑ risk of lichenoid rxn to D-Penicillamine Lichen Planopilaris - scalp only Graham-Little-Picardi-Lasseur Syndrome - scalp & hairbearing body sites Females > Males 4:1 Tufts of normal hair appear in cicatricial areas of alopecia Perifollicular erythema and keratotic spiny papules Tx: Difficult, IL or oral steroids, antimalarials. Interface dermatitis with “saw-tooth” pattern of epidermal hyperplasia together with orthokeratosis and hypergranulosis. Basal layer is lost or “squamatized” with vacuolar interface change, necrotic keratinocytes. “Bandlike” infiltrate in the papillary dermis. “Civatte bodies” are necrotic keratinocytes in the dermis Hyperkeratosis, irregular (saw-tooth) acanthosis, dyskeratosis, basal vacuolization, and a band-like infiltrate of mononuclear cells LICHEN PLANOPILARIS LP Pathology • Hypertrophic LP = LP + LSC • LPP and GLPL = LP histology centered on follicular epithelium • Civatte bodies reveal IgM on DIF • Lichenoid drug reaction may mimic LP. Look for eosinophils, photodistribution Lichen Planus Treatment • Prednisone, Isotretinoin • PUVA, LMW Heparin, Cyclosporine • Oral: potent topical steroids in Orabase w/ vinyl dental tray TID and 20 mins qHS • Plaquenil 400mg daily • Vaginal: mix steroids with Replens (bioadhesive moisurizer) Lichen Planus Actinicus • • • • • MC Africa, Middle East, Indian, Asians MC Spring, Summer, Quiescent in Winter Photodistributed Mild or no pruritis Hyperpigmented macules or plaques with the blue-gray tinge of dermal melanin • May resemble Melasma Erythema Dyschromicum Perstans Erythema Dyschromicum Perstans • Onset before age 40. • Chronic generalized, symmetrical • Various sizes & shapes, ashy-gray macules, sometimes with a palpable nonscaling border. Feels “like a small cord” • Histology: lichenoid infiltrate with pigment laden macrophages in the dermis • Clofazimine helpful. Lichenoid Contact Dermatitis • Dorsal hands - Paraphenylenediamine (color film) • Oral due to Amalgan fillings • Patch testing recommended Keratosis Lichenoides Chronica • Rare, acral & buttocks, onset childhood • Violaceous papulonodular, hyperkeratotic lesions covered with gray scales; discrete or may coalesce to form reticulate or linear arrays, keratotic plugs and prominent telangiectasias • Associated facial “seb derm” pattern • Nail thickening, longitudinal ridging, onycholysis, warty periungual lesions • Painful oral apthae, keratoconjunctivitis Keratosis Lichenoides Chronica Lichen Nitidis Minute, shiny, flat-topped, pale, exquisitely discrete, uniform papules Lichen Nitidis – H&E CHARACTERISTIC PATH: EPIDERMIS GRASPS LYMPHOHISTIOCYTIC INFILTRATE WITH “CLAW-LIKE COLLARETTE LICHEN NITIDIS • Lichen Nitidis • Linear Koebnerization • Lower abdomen and penis, inner thighs, flexor wrists and forearms • Actinic Lichen Nitidis in black, Middle Eastern and Indian subcontinent • Slowly progressive with tendency to remissions • Tx: Top. Steroids, PUVA, DNCB, Oral Retinoids Lichen Striatus • Common, Linear, erythematous or hypopigmented papules, scaly, asymptomatic, follow Blaschko’s lines, nails may be involved • Children age 3, females > males • Active lesions last for months, then resolve • Histology varies, lichenoid or spongiotic, possibly even granulomatous. Dense eccrine infiltrate helps differentiate from LP Lichen Sclerosis et Atrophicus • Females > Males, Itching may be severe • Anogenital “hourglass” or “figure eight” with dyspareunia • Glans penis (balanitis xerotica obliterans) • Chest, breasts, back, oral mucosa, tongue • Histology may have features of morphea • Genital SCC risk higher than general population, but lifetime risk is < 5% LS&A IN A PERIUMBILICAL SKIN FOLD LS&A Etiology • Unknown. • Borrelia burgdorferi assoc. Japan, Europe • 20% of pts have autoimmune disease, usually vitiligo, alopecia areata or thyroid Childhood LS&A • Childhood onset in 10-15%, usually genital • Boys present with phimosis, circumcision may improve/resolve • Girls present with pain with defecation, dysuria and 50% have spontaneous resolution LS&A Histology LATE LS&A: RETE RIDGES EFFACED, EDEMA “FADED, WASHED OUT LOOK”, TELANGIECTATIC VESSELS • JAAD, Volume 48, Number 6: Pages 935-937, June 2003 Tacrolimus ointment for the treatment of vulvar lichen sclerosis. • • Assmann T, Becker-Wegerich P, Grewe M, Megahed M, Ruzicka T. Department of Dermatology, Heinrich-Heine-University, Düsseldorf, Germany. • The treatment of vulvar lichen sclerosus is generally considered difficult. Ultrapotent corticosteroids represent the most effective topical treatment, but carry the risk of side effects such as skin atrophy. We describe a 71-year-old woman with long-standing vulvar lichen sclerosus refractory to conventional treatment. After 6 consecutive weeks of treatment with tacrolimus ointment 0.1% (Protopic) twice daily, signs and symptoms of lichen sclerosus resolved. To our knowledge, this is the first report of the use of topical tacrolimus, which does not induce skin atrophy, in the treatment of vulvar lichen sclerosus. • PMID: 12789187 [PubMed - indexed for MEDLINE] The End