From The Corners Of The World: Geographical Branding: Botanicals - Nutraceuticals World From the Corners of the World: Geographical Branding: Botanicals Regional movements can help communities retain the knowledge and value of their natural resources. By Paul Altaffer & Grant Washington-Smith In the final chapter of our series on regional branding, the focus wil shift to some example
Tablets-au.com Available ED Pharmacy is an 1st. pharmacy providing a individual service to the community in Australia. Over 80,000 extremely satisfied customers! We're your medication drug store cialis australia and have provided trusted service to families in Australia for over 15 years.
Received: December 17, 2001Accepted: February 24, 2002 Meyerson Phenomenon within a
The Different Eczematous Reactions within Port-Wine Stains
on the anteromedial aspect of the left lower localized to the neck and face. They are rare- leg (fig. 1). Further physical examination re- ly found in the context of a Klippel-Trenau- vealed no other skin abnormalities. The pa- nay syndrome . The pathogenesis of this tient does not have any varicose veins. The investigation with color duplex sonography (Sonoline Versa Pro®, Siemens, Linear Ar- Abstract
first time a papulosquamous halo dermatitis ray 5,0L45) did not reveal any insufficient overlying pigmented nevi. Unlike the more perforating vein under the nevus flammeus.
tions overlying nevi flammei exist. All of frequently observed halo nevus or nevus Sut- On histological examination focal acantho- ton, the nevus remains unchanged after the sis, parakeratosis and spongiosis were found scription of an eczematous reaction within a overlying some capillary ectasias. There was congenital nevus flammeus on the left lower 1988, Nicholls and Mason  proposed the no inflammatory infiltrate (fig. 2). Topically leg of a male adult gives reason to discuss eponym ‘Meyerson’s nevus’. Since then, this, also called ‘Meyerson phenomenon’ , has eczema within 2 weeks. Until today no re- rarely been seen in relation with other skin may mostly be a collision dermatosis with tumors [7, 8]. In those cases, the pathogene- an atopic dermatitis, especially when they arise in children and are localized to the neck Discussion
and face. When they are observed within a reported who developed an eczematous reac- grossly visible vascular malformation, as for tion within a congenital nevus flammeus on his left lower leg. A possible relation between vascular structures are common. They most- drome, they may have a pathogenesis simi- this observation and the Meyerson phenom- ly arise as stasis dermatitis from varicose lar to stasis dermatitis. In rare cases, an veins. They can electively be located to der- mal varicose venectasias, but are more often less circumscribed. Histological examina- cism and is interpreted as a variant of the Case Report
tion shows either a subacute or chronic der- matitis with hemosiderin scattered through the dermis, and the dilated vessels are em- bedded in a fibrotic dermis . The patho- flammeus on his left lower leg for 1 year. He genesis of stasis dermatitis is not yet com- Introduction
hardly complained about itchiness. His per- sonal medical history was uneventful. There All the recently reported cases involving was no history of eczema or allergy. Physical matory or eczematous skin changes limited examination revealed a brown reddish area, flammeus, occurred in children [1–3]. They to the area of port-wine stains or congenital about 12 cm in diameter with a pronounced are mostly localized to the neck (otherwise nevi flammei [1, 2]. These observations are and scaly margin, within a nevus flammeus also called salmon patch of the midline) and Tel. +41 56 427 27 22, Fax +41 56 427 00 12, E-Mail email@example.com face. Sidwell et al.  suggest that it may becaused by an abnormal production of cyto-kines, resulting in inflammatory changeswithin the skin. It is also possible that theendothelial cells could play an importantrole in the inflammatory process. Since theeczema improves by laser therapy to theport-wine stains [1, 3], Sidwell et al.  sup-pose that the increased vasculature predis-poses to the development of eczema. AlsoBonifazi and Mazzotta  suppose, that‘.the vascular malformation, with the rele-vant vasodilatation, may be the localizationfactor of the inflammatory changes.’. If thiswere the explanation for this observation,should it not also be possible to find an ecze-ma more frequently within nevi flammei ofadults or within port-wine stains otherwiselocalized than the head, or even also overly-ing the ‘couperose’ of patients with rosacea?Furthermore nuchal nevus flammeus isfound in 15.6% of newborns . Atopiceczema in children and adolescents is local-ized in 10.2% on the nape and in 30.8% onthe neck . Therefore the coincidence of Fig. 1. Eczema (
could also be interpreted as the result of astatistical probability. Eczema taking placewithin a grossly visible vascular malforma-tion , as in the Klippel-Trenaunay syn-drome with arteriovenous anastomoses andvaricose vein segments, may have a patho-genesis comparable to stasis dermatitis. Un-fortunately the reports of Sidwell et al. and Bonifazi and Mazzota  lack any infor-mation about a histological examination.
first time a papulosquamous halo dermatitisoverlying pigmented nevi. Histological ex-amination shows an irregular acanthosis, pa-rakeratosis and focal spongiosis overlying anotherwise unchanged nevus. There are noinflammatory cells invading the pigmentednevus. A lymphocytic perivascular infiltrateis present just peripheral to the nevus. Un-like the more frequently observed halo nevusor nevus Sutton, the nevus remains un-changed, after the inflammatory process hasdisappeared. In 1988, Nicholls and Mason proposed the eponym ‘Meyerson’s ne-vus’. Since then, the ‘Meyerson phenome-non’ , also called ‘nevocentric’ halo der-matitis , has rarely been seen in relationwith other skin tumors [7, 8] or inflammato-ry skin diseases such as atopic eczema (ownobservation), pityriasis rosea , erythemamultiforme  and psoriasis . Even if Fig. 2. On histological examination, focal acanthosis, parakeratosis and spongiosis overlying
an immunological process is suggested [16– some capillary ectasias are seen. There is no inflammatory infiltrate. HE. !100.
18], the exact pathogenesis of this phenome-non has yet to be clarified.
the more pronounced linear lesions reflect that endothelial cells, arranged in monoclon- flammeus does not loose its hair, whereas the al zones, ‘. may be involved in the patho- surrounding skin is undergoing an autoim- genesis of hitherto poorly understood dis- tion of what we call a nevus: ‘Nevi are visi- mune reaction giving rise to alopecia areata.
eases . for example, vascular clones in the ble, circumscribed, long-lasting lesions of the dermis regulate the behavior of epidermal skin or the neighboring mucosa, reflecting quired skin diseases, inflammatory dermati- melanocytes’. Their hypothesis tried to ex- tis or drug eruptions following the Blaschko plain a harlequin-like pattern of skin pig- melanocytic nevi, they do not show neoplas- lines – skin reactions like the Meyerson phe- mentation in a Negress, which we nowadays tic growth. They never show malignant neo- nomenon occurring in the context of nevi, would describe as a patient with chimerism, plasia’ . He supposes that nevi, as a are also the result of genetic mosaicism. The result of their genetic mosaicism, show a here presented 46-year-old man has an ecze- checkerboard, but also including ovoid lenti- matous reaction, strongly limited to the area ginous macules, with their long axes orien- that of the surrounding skin. This genetic of a congenital nevus flammeus on his left tated along the lines of Blaschko. Congenital, mosaic may for instance explain the protec- nevoid and acquired skin diseases following tion of a hairy pigmented nevus from hair show any further abnormalities. There is no the Blaschko lines are thought to be caused loss, whereas the surrounding skin is un- causative varicose vein detectable. The his- by genetic mosaicism, resulting from lyoni- dergoing an autoimmune reaction giving rise tological picture resembles the description zation in X-linked disorders, postzygotic so- to alopecia areata . In 1972, Burgoyne matic mutations in sporadic conditions and  also described a female patient with alo- reaction is interpreted as a new variant of the gametic half-chromatid mutations . In pecia areata: treatment with local injection 2000, Lipsker et al.  demonstrated for of triamcinolone diacetate was followed by the first time that also an acquired inflam- regrowth of hair at the sites injected, but changes within a port-wine stain may mostly matory dermatitis in Blaschko-linear distri- after a time the hair in these areas fell out, be a collision dermatosis with an atopic der- except in the area of a nuchal nevus flam- matitis, especially when they arise in chil- genetic concept, loss of heterozygosity in hu- meus. Port-wine stains fulfil the new defini- dren and are localized to the neck and face. If man skin, plays a role not only in cutaneous tion of a nevus, even if their genetic mosai- they are observed within a grossly visible malignant growth but also in the develop- cism is not yet proved: they are visible, cir- vascular malformation, as for example the ment of benign skin disorders . It may cumscribed, long-lasting lesions. They may also be the explanation for the coexistence of have a pathogenesis similar to stasis derma- a linear and disseminated drug eruption: the  and enhance vascular proliferation [28, titis. In both cases, histological examination loss of heterozygosity in a somatic cell, dur- 29] but they do not show neoplastic growth.
has yet to be done. Further in rare cases, as in ing early embryogenesis, gives rise to a clonal population of cells being either homozygous flammei, similar to melanocytic nevi, as a within a nevus flammeus may be the result result of their genetic mosaicism, show a of genetic mosaicism and is interpreted as a variant of the so-called Meyerson phenome- would reflect a heterozygous state, whereas that of the surrounding skin. This presump- References
1 Tay YK, Morelli J, Weston WL: Inflammatory 8 Gallais V, Lacour J-P, Perrin C, Halioua B, 12 Kissling S, Wüthrich B: Localizations, manifes- nuchal-occipital port-wine stains. J Am Acad Ortonne JP: Halo eczématiforme autour d’un tations and micromanifestations of atopic der- histiocytofibrome: phénomène de Meyerson.
matitis in young adults: Personal follow-up 20 2 Bonifazi E, Mazzotta F: Inflammatory nuchal- Ann Dermatol Vénéréol 1993;120:617–620.
years after diagnosis in childhood. Hautarzt occipital port-wine stains (letter). J Am Acad 9 Lever WF, Schaumburg-Lever G: Noninfec- tious vesicular and bullous diseases; in Lever 13Pariser RJ: ‘Nevocentric’ erythema multi- 3Sidwell RU, Syed S, Harper JI: Port-wine WF, Schaumburg-Lever G (eds): Histopatholo- stains and eczema. Br J Dermatol 2001;144: gy of the skin, ed 6. Philadelphia, Lippincott, 14 Crovato F, Nazzari G, Gambini C, Massone L: 10 Ramelet AA, Monti M: Cutaneous complica- Meyerson’s naevi in pityriasis rosea. Br J Der- eruption involving pigmented nevi. Arch Der- tions related to venous insufficiency; in Ramel- et AA, Monti M (eds): Phlebology: The Guide.
15 Botev IN: ‘Nevocentric’ dermatoses (letter). J Paris, Editions scientifiques et médicales Else- around a melanocytic naevus: Meyerson’s nae- 16 Fernandez Herrera JM, Aragües Montanes M, vus. Br J Dermatol 1988;118:125–129.
11 Camacho F, Navas J: Nuchal nevus flammeus Fraga Fernandez J, Diez CA: Halo eczema in 6 Worret WI: Halo-Ekzeme um Nävuszellnävi in alopecia areata. Dermatology 1992;184: melanocytic nevi. Acta Derm Venereol 1988; (Meyerson-Nävi). Hautarzt 1990;41:262–264.
7 Tegner E, Björnberg A, Jonsson N: Halo der- 17 Feal-Cortizas C, Vargas-Diez E, Buezo GF, matitis around tumours. Acta Derm Venereol Aragües M: Meyerson’s nevus immunohisto- chemical findings in two cases (abstract). Aus-tralas J Dermatol 1997;38(suppl 2):222.
18 Krischer J, Pechère M, Salomon D, Harms M, 22 Happle R: Loss of heterozygosity in human 26 Burgoyne JS: Regrowth of hair in nevus flam- Chavaz P, Saurat JH: Interferon alfa-2b-in- skin. J Am Acad Dermatol 1999;41:143–161.
duced Meyerson’s nevi in a patient with dys- 23Happle R, Effendy I: Coexisting linear and dis- 27 Klapman MH, Yao JF: Thickening and nod- plastic nevus syndrome. J Am Acad Dermatol seminated drug eruption: A clinical clue to the ules in port-wine stains. J Am Acad 2001;44: understanding of the genetic basis of drug erup- 19 Goudie RB, Spence JC, Scothorne RJ: Do vas- 28 Burg G: Collision dermatosis: Angiolymphoid cular clones determine developmental pat- 24 Happle R: What is a nevus? A proposed defini- hyperplasia with eosinophilia developing with- tion of a common medical term. Dermatology in a congenital port-wine nevus. Dermatology 20 Bolognia JL, Seth JO, Glick SA: Lines of Blaschko. J Am Acad Dermatol 1994;31:157– 25 Bon MA, Happle R, Itin PH: Renböck phe- 29 Kim TH, Choi EH, Ahn SK, Lee SH: Vascular tumors arising in port-wine stains: Two cases of 21 Lipsker D, Cribier B, Girard-Lemaire F, Flori pyogenic granuloma and a case of acquired E, Grosshans E: Genetic mosaicism in an ac- tufted angioma. J Dermatol 1999;26:813–816.
quired inflammatory dermatosis following thelines of Blaschko. Arch Dermatol 2000;136:805–807.
Information for Patients Priority Objectives: Via European parents and thus via the Soci- and Interested People ety for Paediatric Nephrologists (ESPN) we have direct contacts to pediatric nephrolo-healing of the very rare, presumably immu-gists in the Netherlands, France, Belgium, nological idiopathic nephrotic syndrome. Evaluation of observational research in or-der to find mor