The use of two substrates for indirect immunofluorescence in the diagnosis of pemphigus

Sir, Sea-urchins are found along the coastline, including in many tourism sites. Their spines consist of calcium carbonate crystals covered by a layer of epithelium. Injuries from seaurchins result from penetration of the spines into the dermis or subcutis, leading to pain of several days' duration. Complications include local inflammation and infection or a delayed granulomatous foreign-body reaction that can develop weeks or months later. The latter may often be followed by long-lasting pain and even by loss of function. To prevent these sequelae, most authors favour the excision of spines rather than waiting for spontaneous recovery as recommended by others. At present, no uniformly accepted successful treatment method is available. We found the erbium:YAG laser to be a suitable tool for effective removal of the spines. Four patients presented to our outpatient department about 1 week after a sea-urchin spinous injury during a vacation. They all suffered from severe pain and loss of function of the injured extremities. Previous attempts to remove the spines mechanically had not been successful. Inspection disclosed multiple black spines (. 50) up to 1 mm in diameter in the soles of the feet (Fig. 1A) in three of the patients. Mobility at the distal interphalangeal joints was reduced due to an accompanying erythematous oedema. The fourth patient had spines in the left index finger, with swelling and reduced flexibility. We decided to use the erbium:YAG laser (Medilas E, Dornier, Munich, Germany; spot size 2 ́5 mm, 300 mJ, fluence 6 J cm, repetition rate 5±10 Hz) to remove the foreign material. Three of the patients were treated under local infiltration anaesthesia (1% lidocaine without epinephrine), and one under general anaesthesia. The foreign bodies were destroyed leaving circumscribed crater lesions with tiny pinpoint areas of bleeding (Fig. 1B). Postoperatively, an antiseptic wound dressing was applied. In two of the patients we took a 2-mm skin biopsy; histological examination revealed penetration of the spines into the deep dermis and even subcutis. Two treatment sessions were necessary to remove all the widespread spines in two patients. The wounds re-epithelialized at the latest within 2 weeks after treatment; in some locations we saw focal hyperkeratosis but there were no signs of scarring. Figure 1(C) shows the typical appearance 4 weeks after treatment. Mobility and function of the distal phalanges were restored completely. During 1 year of follow-up no delayed granulomatous foreign-body reactions or other complications have been observed. Sea-urchins are relatively sedentary creatures often attached to rocks or corals. The porous spines penetrate the skin when stepped on. Mechanical extraction is almost ineffective because the spines fragment easily; surgical excision has been recommended, even though this is difficult with widespread injuries. Leaving spines in place leads to acute pain, local inflammation or infections and a risk of delayed granulomatous foreign-body reactions. There are reports of granulomatous inflammation in the dermis and subcutaneous tissues, with severe involvement of bone and cartilaginous surfaces followed by chronic pain and even loss of function.

[1]  S. Lindahl Academic medicine sets focus on clinical research , 2000, The Lancet.

[2]  P. Lázaro,et al.  Kaposi’s sarcoma‐like lesions and other nodules as cutaneous involvement in AIDS‐related visceral leishmaniasis , 2000, The British journal of dermatology.

[3]  Y. Kameyoshi,et al.  Food‐dependent exercise‐induced anaphylaxis: a report of two cases and determination of wheat‐γ‐gliadin as the presumptive allergen , 2000, The British journal of dermatology.

[4]  T. Olivry,et al.  Anti-plakin and Desmoglein Autoantibodies in a Dog with Pemphigus Vulgaris , 2000, Veterinary pathology.

[5]  S. Challacombe,et al.  A study of desmoglein 1 autoantibodies in pemphigus vulgaris: racial differences in frequency and the association with a more severe phenotype , 2000, The British journal of dermatology.

[6]  J. L. Rees Genetics, past and present, and the rise of systems dermatology , 2000, The British journal of dermatology.

[7]  S. Challacombe,et al.  The use of two substrates to improve the sensitivity of indirect immunofluorescence in the diagnosis of pemphigus , 2000, The British journal of dermatology.

[8]  A. Parodi,et al.  Normal anagen effluvium: a sign of pemphigus vulgaris , 2000, The British journal of dermatology.

[9]  S. Challacombe,et al.  Diagnosis of pemphigus by ELISA: a critical evaluation of two ELISAs for the detection of antibodies to the major pemphigus antigens, desmoglein 1 and 3 , 2000, Clinical and experimental dermatology.

[10]  D. Chakraborti,et al.  Groundwater arsenic contamination in Bangladesh and West Bengal, India. , 2000, Environmental health perspectives.

[11]  T. Nishikawa,et al.  Use of autoantigen-knockout mice in developing an active autoimmune disease model for pemphigus. , 2000, The Journal of clinical investigation.

[12]  G. Block,et al.  Will genetics revolutionize medicine? , 2000, The New England journal of medicine.

[13]  A. Ohta [Adult Still's disease]. , 2000, Ryoikibetsu shokogun shirizu.

[14]  Saurat,et al.  Adult‐onset Still's disease with persistent plaques , 1999, The British journal of dermatology.

[15]  H. Keskinen,et al.  A novel wheat gliadin as a cause of exercise-induced anaphylaxis. , 1999, The Journal of allergy and clinical immunology.

[16]  T. Nishikawa,et al.  The clinical phenotype of pemphigus is defined by the anti-desmoglein autoantibody profile. , 1999, Journal of the American Academy of Dermatology.

[17]  Komai,et al.  Usefulness of enzyme‐linked immunosorbent assay using recombinant desmogleins 1 and 3 for serodiagnosis of pemphigus , 1999, The British journal of dermatology.

[18]  H. Kurzen,et al.  Compositionally different desmosomes in the various compartments of the human hair follicle. , 1998, Differentiation; research in biological diversity.

[19]  R. Prior,et al.  Comparison of different analytical methods for assessing total antioxidant capacity of human serum. , 1998, Clinical chemistry.

[20]  Hughes,et al.  Urticaria as a presentation of adult Still's disease , 1998, The British journal of dermatology.

[21]  R. Lavker,et al.  Desmoglein 3 anchors telogen hair in the follicle. , 1998, Journal of cell science.

[22]  W. Jurecka,et al.  Linear focal elastosis (elastotic striae): increased number of elastic fibres determined by a video measuring system , 1997, The British journal of dermatology.

[23]  J. Savolainen Baker's asthma: diversity of allergens , 1997, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[24]  M. Harth,et al.  Liver transplant in adult Still's disease. , 1997, The Journal of rheumatology.

[25]  J. Sundberg,et al.  Vesicle formation and follicular root sheath separation in mice homozygous for deleterious alleles at the balding (bal) locus. , 1997, The Journal of investigative dermatology.

[26]  N. Akritidis,et al.  Very high serum ferritin levels in adult-onset Still's disease. , 1997, British journal of rheumatology.

[27]  K. Kalimo,et al.  Life‐threatening, recurrent anaphylaxis caused by allergy to gliadin and exercise , 1997, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[28]  G. Patnaik,et al.  Depletion of reduced glutathione, ascorbic acid, vitamin E and antioxidant defence enzymes in a healing cutaneous wound. , 1997, Free radical research.

[29]  J J Strain,et al.  The ferric reducing ability of plasma (FRAP) as a measure of "antioxidant power": the FRAP assay. , 1996, Analytical biochemistry.

[30]  K. Hurlbut,et al.  Mobilization of heavy metals by newer, therapeutically useful chelating agents. , 1995, Toxicology.

[31]  Saha Chronic Arsenical Dermatoses From Tube- Well Water In West Bengal During 1983-87 , 1995 .

[32]  M. Kahn,et al.  Serum ferritin and isoferritins are tools for diagnosis of active adult Still's disease. , 1994, The Journal of rheumatology.

[33]  R Hibst,et al.  Cutting and skin-ablative properties of pulsed mid-infrared laser surgery. , 1994, The Journal of dermatologic surgery and oncology.

[34]  S. Kaur,et al.  Persistent dermal plaque lesions in adult onset Still's disease. , 1994, Dermatology.

[35]  V. Sehgal,et al.  Perforating Dermatoses: A Review and Report of Four Cases , 1993, The Journal of dermatology.

[36]  P. Néve,et al.  Hyperferritinemia in adult onset Still's disease and the hemophagocytic syndrome. , 1992, The Journal of rheumatology.

[37]  H. Sjöström,et al.  Purification and characterisation of antigenic gliadins in coeliac disease. , 1992, Clinica chimica acta; international journal of clinical chemistry.

[38]  A. Pezzutto,et al.  Evaluation of serum ferritin as a marker for adult Still's disease activity. , 1992, Annals of the rheumatic diseases.

[39]  M. Akizuki,et al.  Preliminary criteria for classification of adult Still's disease. , 1992, The Journal of rheumatology.

[40]  J. Patterson,et al.  ULTRASTRUCTURAL CHANGES IN ACQUIRED PERFORATING DERMATOSIS , 1992, International journal of dermatology.

[41]  L. McWilliam,et al.  Spinous injury caused by a sea urchin. , 1991, Journal of clinical pathology.

[42]  J. Esdaile,et al.  Adult Still's Disease: Manifestations, Disease Course, and Outcome in 62 Patients , 1991, Medicine.

[43]  R. Phelps,et al.  Regional variation in the expression of pemphigus foliaceus, pemphigus erythematosus, and pemphigus vulgaris antigens in human skin. , 1991, The Journal of investigative dermatology.

[44]  K. Tadokoro,et al.  Food-dependent, exercise-induced anaphylaxis: a study on 11 Japanese cases. , 1991, The Journal of allergy and clinical immunology.

[45]  R. S. Padilla,et al.  Linear focal elastosis (elastotic striae). , 1989, Journal of the American Academy of Dermatology.

[46]  J. Dormandy,et al.  Causes of venous ulceration: a new hypothesis. , 1989, British medical journal.

[47]  M. Gordon,et al.  Dermatophilus congolensis and "hairy" leukoplakia. , 1988, American journal of clinical pathology.

[48]  M. Al-Ahdal,et al.  Pitted keratolysis: a manifestation of human dermatophilosis. , 1988, Dermatologica.

[49]  A. Ohta,et al.  Adult Still's disease: review of 228 cases from the literature. , 1987, The Journal of rheumatology.

[50]  M. Sabolinski,et al.  Substrate specificity of anti-epithelial antibodies of pemphigus vulgaris and pemphigus foliaceus sera in immunofluorescence tests on monkey and guinea pig esophagus sections. , 1987, The Journal of investigative dermatology.

[51]  J. Graziano Role of 2,3-Dimercaptosuccinic Acid in the Treatment of Heavy Metal Poisoning , 1986, Medical toxicology.

[52]  T. Aoki,et al.  Masked type I wheat allergy. Relation to exercise-induced anaphylaxis. , 1985, Archives of dermatology.

[53]  K. Saha Melanokeratosis from arsenic contaminated tubewell water. , 1984, Indian journal of dermatology.

[54]  S. Benito Urbina,et al.  [Still's disease in the adult]. , 1983, Revista clinica espanola.

[55]  C. Burkhart Pitted keratolysis: a new form of treatment. , 1980, Archives of dermatology.

[56]  H. Mescon,et al.  Comparison of different epithelial substrates useful for indirect immunofluorescence testing of sera from patients with active pemphigus. , 1979, The Journal of investigative dermatology.

[57]  W. F. Lever,et al.  Correlation of antibodies in skin and serum with disease severity in pemphigus. , 1979, Archives of dermatology.

[58]  L. Rubel Pitted keratolysis and Dermatophilus congolensis. , 1972, Archives of dermatology.

[59]  W. Bungeler [Arsenic cancer]. , 1958, Munchener medizinische Wochenschrift.

[60]  E. Bywaters,et al.  The rash of rheumatoid arthritis and Still's disease. , 1956, The Quarterly journal of medicine.

[61]  E. Heilman,et al.  Degenerative Diseases and Perforating Disorders , 2022 .