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Lupus http://lup.sagepub.com/ Dermatologist versus rheumatologist in the management of lupus patients : This debate between father (PF) and daughter (RF) is purely fictional, but it could have easily happened RD Fritsch-Stork and PO Fritsch Lupus 2010 19: 1153 DOI: 10.1177/0961203310370047 The online version of this article can be found at: http://lup.sagepub.com/content/19/9/1153 Published by: http://www.sagepublications.com Additional services and information for Lupus can be found at: Email Alerts: http://lup.sagepub.com/cgi/alerts Subscriptions: http://lup.sagepub.com/subscriptions Reprints: http://www.sagepub.com/journalsReprints.nav Permissions: http://www.sagepub.com/journalsPermissions.nav Citations: http://lup.sagepub.com/content/19/9/1153.refs.html Downloaded from lup.sagepub.com at UNIV N CAROLINA CHAPEL HILL on May 24, 2011 Lupus (2010) 19, 1153–1155 http://lup.sagepub.com VIEWPOINT Dermatologist versus rheumatologist in the management of lupus patients This debate between father (PF) and daughter (RF) is purely fictional, but it could have easily happened PF: Sometimes, medical disciplines behave like belligerent petty medieval states, trying to snatch territories from their neighbours and drive away a few herds of sheep and cattle. Dermatology has always been an easy prey for such waylaying activities – I could give you examples. Rheumatology appears to be another marauder, if you continue to argue that lupus erythematosus (LE) and the other ‘collagen vascular diseases’ rightfully belong to your specialty. RF: My approach is less martial but rather more practical and efficient. Patients should be taken care of by those who can handle them best. There is little doubt that rheumatologists are specialists in systemic immunological diseases, which makes them the first choice to manage an illness such as systemic LE. PF: LE is ‘interdisciplinary’, as are the other collagen vascular diseases. Thus, it is nonsense to allot LE to just one medical discipline – dermatology never laid claims of this kind. The canon of medical disciplines is just an attempt to sort diseases out according to common features. The traditional parameter was the organ most commonly afflicted. This organ system-based canon is simple and straightforward, but it obviously does not do justice to systemic diseases where more than one organ system is involved. Also, the ‘borders’ of disciplines are always fuzzy Correspondence to: Dr Ruth D Fritsch-Stork, Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands. Email: [email protected] due to varying traditions, differences in healthcare systems, and to the impact of dominating personalities at individual institutions. RF: In my view, a new approach of organizing diseases is emerging based on common features of pathogenesis and of shared diagnostic and therapeutic strategies. ‘Thematic’ specialties are being established such as oncology or rheumatology/ clinical immunology. A better understanding of the underlying mechanisms has compelled doctors to think out of their ‘organ system’ boxes. I guess this was the way of thinking which led Kaposi1 to detect the systemic nature of LE, and it is certainly why some of our current treatment options were ‘borrowed’ from other specialties, such as oncology, haematology, transplant medicine . . . PF: . . . and dermatology, for that matter – don’t forget that dermatology used methotrexate some time before the rheumatologists did. There is another point: the ‘organ system’ box is deeply rooted in the minds of the people and in the health systems. Patients who suffer from trouble with one special organ will always attend the respective specialist, and I guess this is not too different even in systems where ‘gatekeepers’ check the patient streams. Dermatologists are responsible for making a diagnosis on patients who seek their advice because of skin problems. LE patients present to the dermatologist with tentative diagnoses of all kinds, such as sunburn, drug eruption, or viral exanthema – but very rarely with ‘suspected LE’. This is even truer for chronic discoid lupus erythematosus (CDLE), which is usually missed as psoriasis by non-dermatologists (and some dermatologists). It is the task of the dermatologist to prove or disprove LE, based on clinical judgment, histopathology (if necessary), and laboratory values. He or she is well equipped for this because the differential diagnosis of LE is one of his/her ! The Author(s), 2010. Reprints and permissions: http://www.sagepub.co.uk/journalsPermissions.nav Downloaded from lup.sagepub.com at UNIV N CAROLINA CHAPEL HILL on May 24, 2011 10.1177/0961203310370047 Dermatologist versus rheumatologist in the management of lupus patients RD Fritsch-Stork and PO Fritsch 1154 core skills. Also, at least in academic centres, histopathology and immunofluorescence labs are at his/her disposal – close clinicopathological interaction is of paramount importance. As a rule, very little help from other specialties, including rheumatology, is needed for a dermatologist to arrive at the diagnosis of LE – by which I mean all forms of LE with cutaneous symptoms, including systemic lupus erythematosus (SLE). RF: Perhaps you overestimate the role of skin signs in SLE. I admit that a lot of SLE patients are sent by dermatologists, which reflects the high percentage of skin symptoms (58–86%).2 However, the number of patients with arthritis and/or vague constitutional symptoms (63–93%, 78–97%)2 is even larger, and only some of them have skin signs. These patients are usually referred to the rheumatologist by primary care physicians, bypassing the dermatologist. The rheumatologist has then to correlate the vague signs and symptoms with concrete physical and laboratory findings for which purpose his/her background as internist serves him/her well, and to obtain consultation from appropriate specialists. Part of this is a visit to the dermatologist, of course. But I doubt if the study of the itinerary of LE patients will carry us any further. By far the bigger role for the rheumatologist is the management of SLE patients. PF: What about the many patients with CDLE, subacute cutaneous lupus erythematosus (SCLE), or ‘latent’ SLE in whom relevant systemic involvement is ruled out? There is no good reason to hand them over to rheumatology or any other specialty because dermatologists are the expert in topical treatment and have decade-long experience in the systemic use of corticosteroids and immunosuppressive agents. Also, rheumatologists would hardly be delighted to be flooded by scores of LE patients displaying nothing but skin lesions. Things are of course different if serious organ involvement is present or emerges later on. It does not take a wise man to say that the patient should then be transferred to where he is best taken care of, even rheumatology. This is quite clear, and all dermatologists I know follow this policy. RF: This might be wise, but I do think it even wiser if any patient with a suspected diagnosis of SLE [e.g. according to the American College of Rheumatology (ACR) criteria] were evaluated by a rheumatologist. The assessment of internal organ involvement critically depends on the focus in history taking, physical examination, and ordering/evaluating the appropriate laboratory tests. And this is a core skill of rheumatology. PF: Did I ever tell you the story of the unfortunate lady who suffered from rosacea and was treated by a rheumatologist for SLE with systemic corticosteroids for more than a year? Dermatological input was considered unnecessary because she had the misfortune of having borderline positive antinuclear antibody (ANA; a common finding in the elderly). My point is – a facial rash plus a positive ANA does not yield the diagnosis of SLE. RF: Well, rheumatologists who overestimate their knowledge may be as bad for patients as dermatologists who do not consult anybody and overlook serositis or nephritis. Everybody should know his/her boundaries – the best service a rheumatologist can provide a lupus patient with solely skin manifestations may be to call the dermatologist. There is no question that dermatology has contributed a lot to the understanding of LE in the past, but more recently, most progress has been made by basic research, often carried out by rheumatologists. PF: There is no doubt on the role of basic research. But I am surprised to hear that you are interested in the history of dermatology. RF: I am interested in the history of LE, and this has been dominated by dermatologists for quite a while – beginning with Willan, Bateman, Cazenave, Biett, Hebra, Kaposi, and many others.3 Not surprisingly, these founding fathers focused mostly (with commendable exceptions!) on the skin signs, of which dermatology continues to discover a bewildering array. PF: They not only discover skin signs, they correlate them with biochemical findings and develop models of pathogenesis, just think of Gilliam and Sontheimer.4 RF: Although the skin manifestations in SLE and their elucidation are important, don’t the systemic symptoms of LE weigh much heavier? And those have been brought to our attention mostly by nondermatologists. Think of Osler, Libman and Sacks, Lupus Downloaded from lup.sagepub.com at UNIV N CAROLINA CHAPEL HILL on May 24, 2011 Dermatologist versus rheumatologist in the management of lupus patients RD Fritsch-Stork and PO Fritsch 1155 Klemperer et al., Hargraves et al., and Friou, to name just a few.5–9 PF: How many rheumatologists are among these non-dermatologists? RF: Rheumatology is a young specialty. The ACR is celebrating its 75th anniversary now, and the first fellowships started only in the 1950s. Thus, rheumatology was not an option for the old guys, unfortunately, although we can guess that they would have chosen it. You should not belittle the impact of rheumatology on the understanding and management of LE. Just consider its role in the characterization of ANA and their subsets,10–12 in the elucidation of the familial occurrence of SLE,12 the (re)discovery of the interferon signature by Crow, Pascual, and Behrends as reviewed by Baechler et al.,14 the institution of a (ACR) classification system,15 and the introduction of corticosteroids in the treatment of SLE.16 PF: Great. But I think you should rather come back to the present and to practical matters. I think we do agree that both dermatology and rheumatology have their own fields of expertise in LE, but we are divided on the issue of who should be responsible for LE with systemic symptoms. Does it suffice to say that everybody should do it who is adequately trained? Whoever takes care of LE, the challenge is not only to make the diagnosis; the patients also need exhaustive information on the disease, the prospects including possible future complications, treatment options, and in depth discussions of necessary life style changes. There is also the need to organize consultations with other medical disciplines, of a detailed treatment schedule, and of appropriate controls. This is the reason why dedicated clinics have been set up in many centres. I do think that these clinics generally work very well, but they must guarantee an interdisciplinary approach. Funding This research received no specific grant from any funding agency in the public, commercial, or not for profit sectors. References 1 Kaposi M. Lupus vulgaris. In: Hebra, F Kaposi M (eds). On Diseases of the Skin including the Exanthemata, Vol IV. Tay W (trans). London: The New Sydenham Society, 1875. 2 Gladman DD, Urowitz MB. Clinical features of systemic lupus erythematosus. In: Hochberg MC, Silman AJ, Smolen JS, Weinblatt ME, Weismann MH (eds), Rheumatology. Philadelphia: Mosby Elsevier; 2007. p. 1277–1297. 3 Hochberg MC. The history of lupus erythematosus. Md Med J 1991; 40: 871–873. 4 Gilliam JN, Sontheimer RD. Subacute cutaneous lupus erythematosus. Clin Rheum Dis 1982; 8: 343–352. 5 Osler W. On the visceral manifestation of the erythema group of skin diseases. Am J Med Sci 1904; 127: 1–23. 6 Libman E, Sacks B. A hitherto undescribed form of valvular and mural endocarditis. Trans Assoc Am Physicians 1924; 38: 46–61. 7 Klemperer P, Baehr G, Pollack AD. Diffuse collagen disease. Acute disseminated lupus erythematosus and diffuse scleroderma. JAMA 1942; 119: 331–332. 8 Hargraves MM, Richmond H, Morton R. Presentation of two bone marrow elements: the ‘tart’ cell and the ‘LE’ cell. Proc Staff Meet Mayo Clin 1948; 23: 25–28. 9 Friou GJ. Clinical application of lupus serum-nucleoprotein reaction using the fluorescent antibody technique. J Clin Invest 1957; 36: 890–895. 10 Holman HR, Kunkel HG. Affinity between the lupus erythematosus serum factor and cell nuclei and nucleoprotein. Science 1957; 126: 162–163. 11 Tan EM, Kunkel HG. Characteristics of a soluble nuclear antigen precipitating with sera of patients with systemic lupus erythematosus. J Immunol 1966; 96: 464–471. 12 Reichlin M. ENA: its place in medicine. Lupus 2002; 11: 201–203. 13 Arnett FC, Shulman LE. Studies in familial systemic lupus erythematosus. Medicine (Baltimore) 1976; 55: 313–322. 14 Baechler EC, Gregersen PK, Behrens TW. The emerging role of interferon in human systemic lupus erythematosus. Curr Opin Immunol 2004; 16: 801–807. 15 Tan EM, Cohen AS, Fries JF, et al. The 1982 revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum 1982; 25: 1271–1277. 16 Hench PS, Kendall EC, Slocumb CH, Polley HF. The effect of a hormone of the adrenal cortex (17-hydroxy-11-dehydrocorticosterone; Compound E) and of pituitary adrenocorticotropic hormone on rheumatoid arthritis. Proc Staff Meet Mayo Clin 1949; 24: 181–197. RD Fritsch-Stork1 and PO Fritsch2 1 RF: ‘Interdisciplinary approach’ is the keyword – after all, our views might not be so far apart. 2 Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, The Netherlands; and Department of Dermatology, University Hospital Innsbruck, Innsbruck Medical University, Austria Lupus Downloaded from lup.sagepub.com at UNIV N CAROLINA CHAPEL HILL on May 24, 2011