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Author: Julianne H Kuflik, MD, Assistant Clinical Professor of Dermatology, Department of Dermatology, UMDNJ-New Jersey Medical School

Julianne H Kuflik is a member of the following medical societies: American Academy of Dermatology

Coauthor(s): Robert A Schwartz, MD, MPH, Professor and Head of Dermatology, Professor of Medicine, Professor of Pediatrics, Professor of Pathology, Professor of Preventive Medicine and Community Health, UMDNJ-New Jersey Medical School

Editors: Noah S Scheinfeld, MD, JD, FAAD, Assistant Clinical Professor, Department of Dermatology, Columbia University; Consulting Staff, Department of Dermatology, St Luke's Roosevelt Hospital Center, Beth Israel Medical Center, New York Eye and Ear Infirmary; Private Practice; David F Butler, MD, Professor of Dermatology, Texas A&M University College of Medicine; Director, Division of Dermatology, Scott and White Clinic; Director Dermatology Residency Training Program, Scott and White Clinic; Van Perry, MD, Assistant Professor, Department of Medicine, Division of Dermatology, University of Texas Health Science Center; Glen H Crawford, MD, Assistant Clinical Professor, Department of Dermatology, University of Pennsylvania School of Medicine; Chief, Division of Dermatology, The Pennsylvania Hospital; Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center

Author and Editor Disclosure

Synonyms and related keywords: AMVC, spontaneously formed facial scars, spontaneous scarring, idiopathic scars, idiopathic scarring, elastic tissue defect, cheek scarring, cheek scars

Background

Atrophia maculosa varioliformis cutis (AMVC) is a rare disease that presents as spontaneously formed facial scars in young adults. In 1918, Heidingsfeld coined the disease name to describe the numerous spontaneously formed scars on the cheeks of a 20-year-old man.

Most commonly located on the cheeks, the scars vary in shape and size, resembling those from smallpox. A slight erythema or pruritus precedes the appearance of the scars by 1-2 days. The number of reports on this eruption in literature is limited, and even fewer are documented with skin biopsy specimens. Its etiology remains unknown, but elastic tissue pathology has been reported in histology findings.

Based on a pedigree assembled by Qu et al and reported in 2005, they suggested that AMVC is of autosomal dominant inheritance.

Pathophysiology

Although its etiology is unknown, AMVC may represent an underlying defect of dermal elastin as demonstrated by histologic and ultrastructural findings. AMVC has been documented only in the skin.

Mortality/Morbidity

In addition to being of cosmetic concern to a patient, the sudden unprecipitated appearance of AMVC causes the patient much anxiety.

Race

No racial predilection is reported.

Sex

The female-to-male ratio is approximately equal.

Age

The reported age range varies from 5-37 years, with the disorder usually appearing in young adulthood.



History

Patients with AMVC deny preceding lesions. They may report a slight erythema or pruritus followed 2 days later by a spontaneously formed scar.

Physical

AMVC may begin with a slight erythema and mild pruritus, followed in 1-2 days by a scar that does not change in size or shape. The shapes of the scars or depressions have been described as linear, round, irregularly round, and varioliform. They are sharply demarcated, flesh-colored shallow depressions of 1 mm subjective depth and may be located bilaterally on the temporal, infraorbital, buccal, mandibular, and mental regions.

  • The most frequently involved sites are the bilateral buccal regions (ie, the cheeks). The scars are almost always located on the face. The length of the scars varies from 2 mm to 1.3 cm, and the width varies from 1-2 mm. These shallow pit marks are arranged parallel, perpendicular, and curvilinear to one another. The depressions are devoid of pigmentary changes from the surrounding skin.
  • Patients usually do not have facial milia, comedones, papules, or cysts. Patients deny a history of scarring secondary to acne or varicella infection, and they deny the presence of a preceding skin lesion, except for the slight erythema that fades upon scar formation. The remainder of their skin examination is unremarkable.
  • Because AMVC can run in families, physical examination of family members may be helpful to rule out a familial disorder and discover other family members with the disease.

Causes

No definitive cause has been established, although skin biopsy specimens for histologic and ultrastructural studies suggest an underlying elastic tissue disorder. Familial cases of AMVC have also been documented. The few associated findings noted were extrahepatic biliary disease and pachydermodactyly.



Anetoderma
Ulerythema

Other Problems to be Considered

Keratosis pilaris atrophicans, including keratosis pilaris atrophicans faciei, or ulerythema ophryogenes; atrophoderma vermiculatum or ulerythema acneiform; and follicularis keratosis spinulosa decalvans

Other common causes of facial scarring, such as a history of varicella zoster virus infection, molluscum contagiosum infection, scarring acne, and herpes virus infection



Procedures

  • A skin biopsy specimen may be sent for histological examination, including special stains for collagen and elastic fibers. An ultrastructural study on the tissue specimen may be considered to help diagnose the disorder and to rule out other diseases in the differential diagnosis.

Histologic Findings

Skin biopsy specimens show decreased or fragmented elastic tissue in the superficial and mid dermis and occasional epidermal thinning or slight epidermal depressions or dells.



Medical Care

No standard of medical care or treatment has been discussed in the literature.



Further Outpatient Care

  • Patients are stable on follow-up visits without treatment. No long-term follow-up data are available.



Medical/Legal Pitfalls

  • Misdiagnoses can occur, particularly if the lesions are diagnosed erroneously as artifactual dermatitis or artifactual scarring. Be careful not to misdiagnose the scars of AMVC as signs of physical abuse, especially in children.



Media file 1:  Atrophia maculosa varioliformis cutis on the cheek presents as curvilinear sharply defined scars or depressions of varying lengths.
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Media type:  Photo

Media file 2:  Histopathology of atrophia maculosa varioliformis cutis shows multiple small areas of diminished and fragmented elastic tissue with Verhoeff-van Gieson stain in the superficial and mid dermis, particularly in the lower aspects of this image.
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo

Media file 3:  Round well-demarcated varioliform scars of atrophia maculosa varioliformis cutis on the temple of the same patient as in Image 1.
Click to see larger pictureClick to see detailView Full Size Image
Media type:  Photo



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Atrophia Maculosa Varioliformis Cutis excerpt

Article Last Updated: Feb 15, 2007