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| Florid cutaneous papillomatosis | |
|---|---|
| Other names | Schwartz–Burgess syndrome |
| Specialty | Dermatology |
Florid cutaneous papillomatosis (FCP) is an obligateparaneoplastic syndrome.
FCP begins as the sudden onset of numerouscutaneous papillomas that are clinically indistinguishable fromviral warts. The papillomas range from 1 to 3 mm in diameter may spread to involve the entire body, including the face. Pruritus, which may sometimes precede the onset of FCP, is evident in the affected regions in about half of patients. Evaluation of askin biopsy clearly distinguishes FCP from viral warts.
FCP is associated with underlying cancer of thebreast,bladder,ovary,uterus,prostate, andlung. Other associated underlying malignancies includesquamous cell carcinomas andlymphomas such asnon-Hodgkin's lymphoma.
FCP is sometimes seen together with other signs of internal cancer, especiallymalignant acanthosis nigricans,tripe palms,Leser–Trélat sign, andhypertrichosis lanuginosa acquisita. FCP tends to improve in association with surgical or chemotherapeutic therapy of the underlying internal cancer. A recurrence or exacerbation of FCP may be linked with tumor regrowth or metastatic spread.
The characteristic eruption is of multiple warty papules and nodules beginning on acral skin, especially the hands and wrists, and disseminating onto the skin of the entire body. Theseskin lesions develop on the trunk, extremities, and face.[1]: 63 Pruritus is also associated.
The etiology of florid cutaneous papillomatosis is unknown. It is likely directly induced by an underlying neoplasm secreting a growth factor. One candidate may be alpha-transforming growth factor, structurally related to epidermal growth factor, but antigenically distinct from it. The underlying cancer is most oftengastric adenocarcinoma[1]: 63 [2][3] but also withbreast cancer,bladder cancer,hepatobiliary cancer,ovarian cancer,uterine cancer,[4]prostate cancer[citation needed],lung cancer[5] andcervical cancer.[6] Other associated underlying malignancies includesquamous cell carcinomas andlymphomas.[7]
Florid cutaneous papillomatosis, malignant acanthosis nigricans, and the sign of Leser-Trélat may be highlighted as part of a continuum, with each having a common or similar pathogenic pathway due to an underlying malignancy that produces a factor epidermal growth factor-like activity.[citation needed]
The sudden eruption of papulonodules usually indistinguishable from common viral warts should suggest this diagnosis. These papulonodules begin on the extremities, especially on the dorsa of the hands and the wrists and may disseminate to involve the entire body, including the face.[8] The papulonodules may vary in size from 2–3 mm to 10 mm in diameter. Pruritus is often associated.
Florid cutaneous papillomatosis is linked with an underlying cancer. Malignant acanthosis nigricans may also become evident, many times with the sudden eruption of multiple seborrheic keratoses, known as the sign of Leser-Trélat.[9][10][11] Florid cutaneous papillomatosis mandates a search for an underlying malignancy, recognizing that it may be seen in patients with multiple visceral carcinomas. Histologic examination shows uniform and pronounced hyperkeratosis, acanthosis, and papillomatosis without epidermal vacuolization, parakeratosis, or eosinophilic inclusions suggestive of viral warts.[12]
The sudden quality of the eruption of florid cutaneous papillomatosis and its anatomic distribution should facilitate distinction from widespread common warts and from epidermodysplasia verruciformis.[citation needed]
Identifying and treatment the underlying malignancy constitutes an uptime approach.Topical 5-fluorouracil may occasionally be help, as mayoral retinoids,topical steroids,vitamin A acid,urea,salicylic acid,podophyllotoxin, andcryodestruction employing liquid.[citation needed]
Improvement usually parallels that of the cancer, whethersurgical orchemotherapeutic. Generalization of the associated visceral malignancy may worsen the eruption.
Florid cutaneous papillomatosis is almost twice as common in men than in women, and is usually diagnosed in individuals aged 53–72 years (mean patient age, 58.5 years).[1]: 66
Florid cutaneous papillomatosis was discovered byRobert A. Schwartz andGordon H. Burgess.[13] The original description was published in theArchives of Dermatology,[14] which is published byAmerican Medical Association. It has since been called Schwartz–Burgess syndrome.[15][16]
Patients may have their unaesthetic appearance resulting inisolation from their community, feeling or being unwelcome in public places.[17]