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PXE and the Primary Care Practitioner

Pseudoxanthoma elasticum (PXE) is a heterogeneous inherited disorder of connective tissue, the hallmark of which is dystrophic calcification of elastic tissue of the skin, retina, and arteries. The primary care physician may be the first to suspect and diagnose PXE because of the varied clinical manifestations involving several body systems. He or she may coordinate the lifelong specialty care of the affected patient, and most importantly, may be expected to be an
authoritative resource as well as source of support for the patient and family.

Skin manifestations
The primary lesion of PXE is a small 2-5 mm yellowish or yellow-orange papule, irregular or rhomboid in shape (hence the term pseudoxanthoma), which may form groups or coalesce into
larger plaques. The lesions are asymptomatic and tend to be distributed symmetrically on flexural areas progressing downward from the neck to the axillae and antecubital fossae, and later to the
groin and popliteal fossa. Less common areas of involvement include the periumbilical area, oral, and anogenital mucosa. Oral lesions, seen on the inner aspect of the lower lip resemble Fordyce
spots.
The lesions may give the affected skin a "plucked chicken" or "cobblestone" appearance. The lesions may cause the skin of the neck to appear unwashed. Differential diagnosis must
consider solar elastosis.
The skin lesions develop during childhood or adolescence, and progress slowly and unpredictably with age, spreading from the neck downward. The neck, axillae, groin, or face may sometimes manifest lax, redundant folds of skin in late stage PXE.
Skin biopsy of lesional (and sometimes non-lesional) skin confirms the diagnosis if it shows calcification of fragmented, clumped elastic fibers in the mid- and lower dermis can confirm the diagnosis. The highest yield is from biopsy of a primary lesion (papule). In the absence of primary lesions, punch biopsy of neck, axilary and/or antecubital fossa are recommended.The skin lesions are asymptomatic. Affected individuals with unsightly redundant folds can undergo cosmetic surgical correction, usually with uncomplicated wound healing, although healing may sometimes be poor or accompanied by calcium extrusion through the wound.
Although skin manifestations are most characteristic of PXE, the ocular and cardiovascular manifestations are responsible for the morbidity of the disease. Indeed, in some cases the skin
lesions are not visible.

Retinal Disease
The earliest, and often subtle, manifestation of PXE in the retina is peau d'orange, a diffuse yellowish mottling of the fundus usually seen in the first two decades of life. The characteristic retinal lesion is the angioid streak, seen in most adult affected individuals, and seen sometimes in children. Angioid streaks are gray to brown or dark red, spoke-like bands radiating out from the optic disc or encircling the disc with peripapillary streaks. Angioid streaks correspond to breaks in Bruch's membrane, an elastin rich layer of the choroid. Neovascular capillary nets can grow through these breaks, leading to hemorrhage. These can lead to central visual loss (not true blindness), if they occur in the macula or fovea. Laser photocoagulation may be effective in obliterating neovascularization, but it often recurs, and disciform scarring can further compromise central vision.

Vascular Disease
The basic vascular pathology in PXE is dystrophic calcification of the elastic tissue of the media. Subsequent intimal elastic calcification and atherosclerosis and intimal fibrous proliferation
leading to vascular occlusion or fragility may occur. The most common manifestations of arterial disease in PXE are diminished peripheral pulses and intermittent claudication. Angina and
symptoms of intestinal ischemia may occur relatively early in life. Hypertension may be more common among affected individuals with PXE. If present, this increases the risk of vascular complication in the individuals affected by PXE, and needs to be well controlled. GI bleeding, usually gastric, may be an early manifestation and even the presenting sign of PXE. The mechanism is unknown, but gastroscopy shows gastric mucosal changes resembling mucosal PXE
elsewhere (yellowish papules), and the histology of the gastric vessels resembles that of other arteries affected by PXE.

Genetics of PXE
PXE may be inherited as either an autosomal recessive or dominant trait. Sporadic cases either represent autosomal recessive transmission, autosomal dominant transmission from an affected parent with minimal or inapparent disease (who might actually represent a heterozygous recessive carrier), or spontaneous dominant mutations. Some recessive carriers may have mild clinical manifestations. Clinical expression is not helpful in predicting the mode of inheritance;
PXE is quite heterogeneous and environmental influences may modify the clinical expression. The gene is on the short arm of chromosome 16 (16p13.1) and codes for the membrane transport
protein, ABCC6. Mutational analysis is in progress, as are functional studies of the gene.

Workup of the Individual Affected by PXE
General workup of the individual affected by PXE should include:
• A history detailing with onset, symptoms of vascular and ocular disease, and family history.
• Examination of the skin and cardiovascular system, including peripheral pulses.
• Confirmation of diagnosis by skin biopsy with appropriate calcium stains.
• Laboratory evaluation of lipids.
• Examination of first degree relatives.

Management of Individuals Affected by PXE
As are most inherited diseases, PXE is incurable. Management should focus on education of the affected individual, genetic counseling, monitoring and treatment of complications, and
dietary and lifestyle modifications to delay or possibly prevent complications. This may involve a team approach including dermatologist, primary care physician, ophthalmologist, cardiologist,
vascular surgeon, plastic surgeon, genetic counselor, nutritionist and support groups. Support groups are of tremendous benefit in helping affected individuals cope with the disorder. The affected individual (or parent) needs to be educated in understandable terms regarding
the various manifestations of the disease and the prognosis (which is not as dire as some affected individuals are led to believe). Offer genetic counseling with caution, as the genetic transmissibility
of the disease is not yet understood. Regular ophthalmologic examination by a physician with expertise in retinal disease is essential, and affected individuals should learn to use the Amsler grid to monitor for central visual disturbances. Regular physical examinations with specific attention to the gastrointestinal and cardiovascular systems are essential. Lipid levels should be monitored periodically.
Surgical intervention may be indicated for gastrointestinal bleeding, severe peripheral vascular disease (if correctable), and the improvement of cosmetic deformities of the face, neck, axilla, and groin. Wound healing seems to be uncomplicated in PXE, although cosmetic acceptability is less predictable.
Weight control, avoidance of smoking, and aggressive management of hypertension and lipid disorders are all essential in delaying or reducing the severity of vascular complications.
Pentoxifylline may be of value in managing claudication. Aspirin and other non-steroidal anti-inflammatory medications should be avoided due to the risk of gastrointestinal hemorrhage. Most women with PXE have normal pregnancies, however gastric or uterine bleeding may
very rarely complicate them. Fetal complications due to impaired uteroplacental blood flow do not appear to be a problem. There is no basis for women affected by PXE to avoid becoming pregnant.
There are at present no tests for prenatal diagnosis of this disease. With characterization of the defective gene and gene products, such tests may eventually become available.
It has been reported that high calcium intake early in life may correlate with the overall severity of PXE, but this has not been confirmed by studies, and remains controversial.
PXE International, Inc. maintains a Blood and Tissue Bank and an international registry.
Please encourage affected individuals to register with them.

Bergen AA, Plomp AS, Schuurman EJ, Terry S, Breuning M, Dauwerse H, Swart J, Kool M, van Soest S, Baas F, ten Brink JB, de Jong PT. Mutations in ABCC6 cause pseudoxanthoma elasticum. 2000 Jun. Nat. Genet. 25, 228-231.

Lebwohl M., Neldner K., Pope F.M. et al: Classification of pseudoxanthoma elasticum. Report of a consensus conference. J Am Acad Dermatol. 1994; 30:103-107. A contemporary clinical
classification that does not depend on heredity.

Le Saux O, Urban Z, Tschuch C, Csiszar K, Bacchelli B, Quaglino D, Pasquali-Ronchetti I, Pope FM, Richards A, Terry S, Bercovitch L, de Paepe A, Boyd CD. Mutations in a gene encoding
an ABC transporter cause pseudoxanthoma elasticum. Nat Genet. 2000 Jun;25(2):223-7. A discussion of the gene defective responsible for pseudoxanthoma elasticum.

Neldner K.H. Pseudoxanthoma elasticum. Clin Dermatol 1988; 6: 1-159. The most encyclopedic review of the subject for the practitioner.
Renie, WA Pyeritz RE, Comb J et al: Pseudoxanthoma elasticum: High calcium intake early in life correlates with severity. Am J Hum Genet 1984;19: 235-244. Overall, severity in both sexes correlate with high calcium intake in early life, but sample size to small to confirm for either sex or individual features of disease. Indeed, correlation was negative for women.

Viljoen D.L., Bloch C, Beighton P: Plastic surgery in pseudoxanthoma elasticum: Experience in nine patients. Plast Reconst Surg.1990; 233-38. A series discussing wound healing and surgical outcomes in a small group of women under going cosmetic surgery of redundant
skin in PXE.

Uitto J, Boyd CD, Lebwohl MG, Moshell AN, Rosenbloom J, Terry S. International Centennial Meeting on Pseudoxanthoma Elasticum: progress in PXE research. J Invest Dermatol. 1998 May; 110 (5):
840-2.

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