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Journal articles on the topic 'Photodermatosis'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 April 2022

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1

LEDO, ELENA. "PHOTODERMATOSIS. PART I: PHOTOBIOLOGY, PHOTOIMMUNOLOGY, AND IDIOPATHIC PHOTODERMATOSES." International Journal of Dermatology 32, no. 6 (June 1993): 387–96. http://dx.doi.org/10.1111/j.1365-4362.1993.tb02805.x.

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2

Murashkin, Nikolay N., Eduard T. Ambarchian, Roman V. Epishev, Alexander I. Materikin, Leonid A. Opryatin, Roman A. Ivanov, and Daria S. Kukoleva. "Photodermatoses in Childhood." Current Pediatrics 20, no. 5 (November 7, 2021): 360–69. http://dx.doi.org/10.15690/vsp.v20i5.2308.

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Photodermatoses is a heterogeneous group of diseases resulting from abnormal skin hypersensitivity to sunlight and presented as local or generalized rashes. Specific sensitivity of children's skin to ultraviolet is often the first sign or clinical symptom of photodermatosis. Abnormal photosensitivity can be represented by diverse group of primary idiopathic conditions or photo-mediated aggravation of existing dermatosis. Number of genetic genodermatoses, metabolic disorders and connective tissue diseases is also widely known. These conditions can manifest with photosensitivity associated to other extracutaneous clinical and laboratory features. Timely diagnosis of photosensitivity in childhood allows to minimize long-term complications associated with insufficient photoprotection.

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3

Delgado, Luis. "Bullous Photodermatosis After Lomefloxacin." Archives of Dermatology 130, no. 6 (June 1, 1994): 808. http://dx.doi.org/10.1001/archderm.1994.01690060146030.

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4

Yanamandra, U., K. K. Sahu, P. Malhotra, and S. Varma. "Photodermatosis secondary to hydroxyurea." Case Reports 2014, sep30 1 (September 30, 2014): bcr2014205974. http://dx.doi.org/10.1136/bcr-2014-205974.

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5

Correia, O. "Bullous photodermatosis after lomefloxacin." Archives of Dermatology 130, no. 6 (June 1, 1994): 808–9. http://dx.doi.org/10.1001/archderm.130.6.808.

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6

Sakaniya, L. R., A. L. Piruzyan, and I. M. Korsunskaya. "Drug reactions in dermatology: photodermatosis." Klinicheskaya dermatologiya i venerologiya 19, no. 4 (2020): 545. http://dx.doi.org/10.17116/klinderma202019041545.

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7

CHERIAN, SHIELA. "IS GRANULOMA MULTIFORME A PHOTODERMATOSIS?" International Journal of Dermatology 33, no. 1 (January 1994): 21–22. http://dx.doi.org/10.1111/j.1365-4362.1994.tb01486.x.

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8

Roelandts, Rik, and Stephanie Ryckaert. "Solar urticaria: the annoying photodermatosis." International Journal of Dermatology 38, no. 6 (June 1999): 411–18. http://dx.doi.org/10.1046/j.1365-4362.1999.00620.x.

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9

Dhillon, K., Tarunveer Singh, Deepak Sharma, K. Varshney, Nikha Garg, Priyanka Priya, Uroos Fatima, and Simmi Chawla. "Hydroa vacciniforme: a very rare photodermatosis." International Journal of Advances in Medicine 1, no. 2 (2014): 1. http://dx.doi.org/10.5455/2349-3933.ijam20140802.

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10

Kuklin, V. T., O. V. Torbin, L. I. Bychkova, D. E. Tsyplakov, and V. R. Gilmutdinova. "Actinic reticuloid case." Kazan medical journal 80, no. 3 (April 2, 1999): 224–26. http://dx.doi.org/10.17816/kazmj66775.

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Actinic reticuloid means a type of photodermatosis, the pathohistological characteristics of which in the skin are identical to those in fungal mycosis and clinically resemble the skin condition of peasants and sailors.

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11

BOSCHERT, SHERRY. "Idiopathic Photodermatosis Is a Dx of Exclusion." Skin & Allergy News 37, no. 10 (October 2006): 31. http://dx.doi.org/10.1016/s0037-6337(06)71597-2.

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12

Belan, E. B. "Solar urticaria." Russian Journal of Allergy 13, no. 6 (December 15, 2016): 11–17. http://dx.doi.org/10.36691/rja345.

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Solar urticaria is defined as relatively rare photodermatosis induced by visible or ultraviolet (A) light. The diagnosis of the disease is based on the anamnesis and phototesting data. Management of the solar urticaria includes dark clothes, sunscreens, non-sedative antihistamines. Alternative interventions may be considered if high doses of non-sedative antihistamines are ineffective.

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13

Jeanmougin, M., and J. Civatte. "Benign summer light eruption: The most common photodermatosis." Journal of the American Academy of Dermatology 17, no. 4 (October 1987): 690–91. http://dx.doi.org/10.1016/s0190-9622(87)80461-9.

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14

ORTON, D. I., S. H. WAKELIN, and S. A. GEORGE. "Brachioradial photopruritus—a rare chronic photodermatosis in Europe." British Journal of Dermatology 135, no. 3 (September 1996): 486–87. http://dx.doi.org/10.1111/j.1365-2133.1996.tb01523.x.

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15

ORTON, D. I., S. H. WAKELIN, and S. A. GEORGE. "Brachioradial photopruritus-a rare chronic photodermatosis in Europe." British Journal of Dermatology 135, no. 3 (September 1996): 486–87. http://dx.doi.org/10.1046/j.1365-2133.1996.d01-1030.x.

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16

Almeida Jr, Hiram Larangeira de, Janaína Kopp, Valeria Magalhães Jorge, Debora Sarzi Sartori, and Carolina Dahmer Velloso. "Extensive hydroa vacciniforme." Anais Brasileiros de Dermatologia 88, no. 4 (August 2013): 620–22. http://dx.doi.org/10.1590/abd1806-4841.20131867.

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Hydroa Vaciniforme is a very rare photodermatosis that is mainly seen in childhood. An 18 year old female student reported that since the age of 5 she has been suffering necrotic lesions and vesicles lesions in exposed areas, leaving asymptomatic varioliform scars, which worsened in summer. Light microscopy showed epidermal necrosis with lymphocytic infiltration . Sunscreens were prescribed with light improvement.

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17

Colebunders, R., Y. Fleerackers, A. Stevens, and P. Van Damme. "Photodermatosis in Association with the Acquired Immune Deficiency Syndrome." International Journal of Dermatology 33, no. 7 (July 1994): 523–24. http://dx.doi.org/10.1111/j.1365-4362.1994.tb02880.x.

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18

Beckman, L., G. Beckman, B. Cedergren, Kerstin Göransson, E. B. Hallqvist, and C. Sikström. "Transferrin C Subtypes and Occupational Photodermatosis of the Face." Human Heredity 35, no. 2 (1985): 89–94. http://dx.doi.org/10.1159/000153522.

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19

Trelles, Andrés Sanz, and Elisabeth Gómez Moyano. "A new case of neutrophilic sebaceous adenitis: A photodermatosis?" Journal of the American Academy of Dermatology 60, no. 5 (May 2009): 887–88. http://dx.doi.org/10.1016/j.jaad.2008.11.004.

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20

Orlov, E. V., and P. E. Konnov. "The role of antihistamines in chronic actinic dermatitis treatment." Vestnik dermatologii i venerologii 92, no. 1 (February 24, 2016): 81–84. http://dx.doi.org/10.25208/0042-4609-2016-92-1-81-84.

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Inveterate actinic dermatitis is an immunologically mediated photodermatosis characterized by itchy eczematous dermhelminthiasis exposed to sunlight. The disease proceeds in the same way as the atopic eczema or atopic dermatitis. The treatment of patients with inveterate actinic dermatitis is similar to the treatment of patients with atopic dermatitis and eczema. Administration of the modern antihistaminic preparation desloratadine (Aerius) in the treatment has a positive effect on the skin process relief and on some cellular and humoral immunity factors.

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21

Ferrer Guillén, Blanca, Laura Cubells Sánchez, JoséLuis Sánchez Carazo, and Amparo Pérez Ferriols. "Adverse cutaneous events after laser epilation in patients with photodermatosis." Indian Journal of Dermatology, Venereology and Leprology 84, no. 6 (2018): 718. http://dx.doi.org/10.4103/ijdvl.ijdvl_581_17.

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22

Patel, Bipin B., Thomas G. Waddell, and Richard M. Pagni. "Explaining photodermatosis: cyclopentenone vs. α-methylene-γ-lactone natural products." Fitoterapia 72, no. 5 (June 2001): 511–15. http://dx.doi.org/10.1016/s0367-326x(01)00257-x.

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23

Helsing, Per, and Joar Austand. "Contact dermatitis mimicking photodermatosis in a 1-year-old child." Contact Dermatitis 24, no. 2 (February 1991): 140–41. http://dx.doi.org/10.1111/j.1600-0536.1991.tb01673.x.

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24

PATEL, GIRISH K., GOULD, HAWK, and JANE M. MCGREGOR. "A complex photodermatosis: solar urticaria progressing to polymorphic light eruption." Clinical and Experimental Dermatology 23, no. 2 (March 1998): 77–78. http://dx.doi.org/10.1046/j.1365-2230.1998.00317.x.

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25

Armstrong, D. K. B., and E. A. Bingham. "Brachioradial Pruritus – An Uncommon Photodermatosis Presenting in a Temperate Climate." Dermatology 195, no. 4 (1997): 414–15. http://dx.doi.org/10.1159/000246007.

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26

Maširević, Iva, Biljana Marenović, Svetlana Popadić, and Miloš Nikolić. "Hydroa Vacciniforme - A Case Report / Hydroa vacciniforme - prikaz slučaja." Serbian Journal of Dermatology and Venerology 4, no. 2 (May 1, 2012): 81–84. http://dx.doi.org/10.2478/v10249-012-0007-6.

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Abstract Hydroa vacciniforme is a rare, idiopathic, chronic photodermatosis that usually begins in childhood and resolves spontaneously in early adulthood. It is characterized by appearance of vesicles on sun-exposed areas. The vesicles crust and heal within one to six weeks, leaving vacciniform/varioliform scars. We report an 11-year-old boy with a 5-year history of recurrent blisters on sun-exposed areas that deteriorated each summer. He was treated with antimalarials, topical photoprotective agents, sun avoidance, dietary fish oil and supplementary doses of vitamin D3. Strict adherence to the regimen resulted in remission.

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27

Aryal, Eliz, Sabina Bhattarai, Govind Pokhrel, and B. Sanju Shrestha. "Photodermatosis and Photo protection in Metropolitan Traffic Police in Kathmandu city." International Journal of Occupational Safety and Health 8, no. 2 (December 31, 2018): 19–24. http://dx.doi.org/10.3126/ijosh.v8i2.23332.

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Background: Police officer serves a vital role in maintaining safety and serve are role model for discipline throughout the world, they are non–intentional type sun exposure(NISE).The objective of our present study was to evaluate photo protector practice, knowledge in response to Ultra violet Radiation ,Sunscreens and sun related photodermatosis. Methodology: A cross sectional study was conducted in traffic police officer at different locations at Kathmandu. Data was collected by using self-administered questionnaires and interviewed by Dermatologist to establish their knowledge and behaviour and practice in relation to ultra violet radiation and photo-protection. Result: Out of 265 participants, mean age was 27.1 years. Respondent with graduation and master degrees had knowledge and practice toward UVR, follow by higher secondary education. Regarding the practice for photo protection only 59.6% had knowledge about sunscreen, 39.6% knowledge about Ultraviolet Radiation and 24.9% had knowledge about Ultra Violet Index .Skin problem like melasma, premature wrinkles, and hardening of skin, polymorphic light eruption, burning foot syndrome, dermatophytes, and varicose vein. Conclusion: Traffic police officers showed good practices in term of wearing hat, clothes that cover most of the body parts but poor practice over sunscreen, UVR, UVI. Lectures & seminar regarding the awareness and photo protection practice should be recommended. With lack of awareness among police officers and providing sunscreen for free should be considered by Police authorities. Similarly lectures & seminar on sun protection should be provided in regularly.

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28

Kirchberger, M., M. Sticherling, and M. Erdmann. "Uncommon Presentation of Scleromyxoedema with a Distribution Pattern Mimicking a Photodermatosis." Acta Dermato Venereologica 97, no. 8 (2017): 979–80. http://dx.doi.org/10.2340/00015555-2684.

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29

Azevedo, Luciana Cirillo Maluf, Carlos D' Aparecida Santos Machado Filho, Maura Simonetti Junqueira de Andrade, Alessandra Bunemer Nahas, and Mellysande Pontes Faccin. "The importance of the dermatologist at the hospital." Anais Brasileiros de Dermatologia 87, no. 3 (June 2012): 501–3. http://dx.doi.org/10.1590/s0365-05962012000300031.

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Skin lesions are often underestimated when patients are hospitalized in clinical or surgical areas. We made weekly visits to Mario Covas State Hospital of Sao Paulo, Brazil, for 35 weeks. Patients answered a questionnaire and underwent skin examination. The skin lesions were photographed. Of the 359 patients evaluated, a total of 1098 dermatological conditions were diagnosed. The most prevalent skin conditions included photodermatosis, neoplasms, vasculopathies and onychopathies. The growing number of dermatological diseases in hospitals justifies the active and constant presence of the dermatologist in a multidisciplinary team, thereby improving prognosis and patients' quality of life.

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30

Weryszko-Chmielewska, Elżbieta, and Mirosława Chwil. "Structures of Heracleum sosnovskii Manden. stem and leaves releasing photodermatosis-causing substances." Acta Agrobotanica 67, no. 4 (2012): 25–32. http://dx.doi.org/10.5586/aa.2014.057.

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In its stems and leaves, <em>Heracleum sosnovskii</em> Manden. contains furanocoumarins, which exert a phototoxic effect on humans. The aim of the investigations was to describe the external secretory structures of the epidermis and internal secretory tissues in organs responsible for emission of secretion that is toxic to human skin. The study was conducted using light and fluorescence microscopy. On the stems and leaves, various types of secretory trichomes with dispersed or deposited secretion were found. The trichomes were most abundant on the abaxial leaf surface. Epidermal cells and the secretion present on the trichomes exhibited intense fluorescence, which may indicate the presence of furanocoumarins in the tissue and trichome secretions.

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31

Bertrand, Janie, Joe T. R. Clarke, and Dominique Hanna. "Erythropoietic Protoporphyria: Spectrum of Three Cases." Journal of Cutaneous Medicine and Surgery 16, no. 5 (September 2012): 311–16. http://dx.doi.org/10.1177/120347541201600507.

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Background: Erythropoietic protoporphyria is a rare photodermatosis of childhood, and the diagnosis can be delayed. A deficient ferrochelatase enzyme leads to accumulation of protoporphyrins in the dermis, causing phototoxic burning. Objective: To report three cases with great variability in severity of symptoms and age at diagnosis. We discuss clinical and biochemical findings, mutation analysis, and therapeutic options. Methods: We report three cases with different degrees of photosensitivity, laboratory results, psychosocial impact, and preventive and therapeutic treatments. Results: The diagnosis of erythropoietic protoporphyria was confirmed by both typical elevation of plasma porphyrins and the discovery of a mutated FECH gene. Conclusion: Erythropoietic protoporphyria should be suspected in any cases of childhood photosensitivity. Systemic complications are unusual. Mutation analysis confirms the diagnosis. Photoprotection is the cornerstone of treatment. Renseignements de base: La protoporphyrie érythropoïétique est une photodermatose infantile rare, et le diagnostic peut être retardé. Une déficience de l'enzyme ferrochélatase produit une accumulation de protoporphyrines dans le derme ce qui provoque une réaction phototoxique. Objectif: Présenter trois cas qui illustrent une grande variabilité de la gravité des symptômes et de l'âge au moment du diagnostic. Nous discutons des résultats cliniques et biochimiques, de l'analyse des mutations, et des options thérapeutiques. Méthodes: Nous exposons trois cas qui présentent différents degrés de photosensibilité, les résultats d'examen de laboratoire, l'impact psychosocial, et les traitements préventifs et thérapeutiques. Résultats: Le diagnostic de la protoporphyrie érythropoïétique a été confirmé à la fois par l'élévation caractéristique des porphyrines plasmatiques et par la mise en évidence d'une mutation du gène FECH. Conclusion: La protoporphyrie érythropoïétique doit être soupçonnée dans tous les cas de photosensibilité infantile. Les complications systémiques sont inhabituelles. L'analyse des mutations confirme le diagnostic. La photoprotection est la pierre angulaire du traitement.

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32

Sardana, Kabir, Khushbu Goel, VijayKumar Garg, Alka Goel, Deepshikha Khanna, Chander Grover, and Nita Khurana. "Is frictional lichenoid dermatitis a minor variant of atopic dermatitis or a photodermatosis." Indian Journal of Dermatology 60, no. 1 (2015): 66. http://dx.doi.org/10.4103/0019-5154.147797.

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33

DENG, Danqi, Yuntao HANG, Hao CHEN, and Hanying LI. "Prevalence of photodermatosis in four regions at different altitudes in Yunnan province, China." Journal of Dermatology 33, no. 8 (August 1, 2006): 537–40. http://dx.doi.org/10.1111/j.1346-8138.2006.00123.x.

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34

Krutmann, Jean. "Ultraviolet A radiation-induced biological effects in human skin: relevance for photoaging and photodermatosis." Journal of Dermatological Science 23 (March 2000): S22—S26. http://dx.doi.org/10.1016/s0923-1811(99)00077-8.

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35

Bissonnette, Robert, Noel Buskard, David I. McLean, and Harvey Lui. "Treatment of Refractory Solar Urticaria with Plasma Exchange." Journal of Cutaneous Medicine and Surgery 3, no. 5 (July 1999): 236–38. http://dx.doi.org/10.1177/120347549900300503.

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Background: Solar urticaria is a photodermatosis that can be very disabling for patients who are highly sensitive to light and can also be very resistant to therapy. Objective: To correlate the results of serial phototesting in a patient with severe and refractory solar urticaria before and after treatment with plasma exchange. Methods: Plasma exchange was performed five times over a period of 10 days. Phototesting to ultraviolet A (UVA) irradiation and visible light was performed with fluorescent ultraviolet tubes and an incandescent lamp. Results: The urticaria that developed after very low light doses during baseline phototesting could not be provoked following plasma exchange. The patient is now almost symptom-free, with only occasional and transient hives more than 21 months after her last plasma exchange. Conclusions: Plasma exchange is a therapeutic modality to consider in highly light-sensitive patients when other treatments have failed.

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36

Gamé, Denise, Juli Bassas, Cristina Grau, Carlos Ferrándiz, and José Manuel Carrascosa. "Fixed sunlight eruption: a new idiopathic photodermatosis rather than a variant of fixed drug eruption." Photodermatology, Photoimmunology & Photomedicine 33, no. 4 (April 26, 2017): 222–24. http://dx.doi.org/10.1111/phpp.12309.

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37

Чоп’як, Валентина, Христина Ліщук-Якимович, Роман Пукаляк, and Омелян Синенький. "ANTISYNTHETASE SYNDROME AND THE POSITION OF CLINICAL IMMUNOLOGIST." Immunology and Allergy: Science and Practice, no. 2 (July 29, 2020): 66–71. http://dx.doi.org/10.37321/immunology.2020.02-07.

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Antisynthetase syndrome is a clinical and laboratory syndrome that develops in patients with idiopathic inflammatory myopathy and is characterized by the development of interstitial lung disease, namely fibrosing alveolitis syndrome, resistance to traditional corticoid therapy and the presence of myositis-specific antibodies.We present a clinical case of an antisynthetase syndrome in a middle-aged patient who has presented severe myalgic syndrome, photodermatosis, Raynaud’s phenomenon. The disease debuted with cutaneous (heliotropic erythema, erythematous rash on the skin of the upper torso) and myalgic symptoms, fever with next adding of the joint syndrome, as well as lung damage (pulmonitis and infiltrates). Immunological testing revealed anti-Jo-1, anti-PL-12-, anti-PL-7 antibodies («Polycheck», BIOCHECK, Germany). Since years, the patient has got the diagnosis of antisynthetase syndrome. The use of combined pulse therapy with cyclophosphamide and methylprednisolone, as well as the addition of high doses of vitamin D3 has contributed to the regression oflung damage and reduction of dermatomyositis activity.

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38

ცისკარიშვილი ნ., Tsiskarishvili N., Katsitadze A. კაციტაძე ა., Tsiskarishvili N. ცისკარიშვილი ნ., Tsiskarishvili Ts ცისკარიშვილი ც., and Chitanava L. ჭითანავა ლ. "PERSPECTIVE OF PHOTOTHERAPY OF DERMATOSES BY MEANS OF UVB -311 NM." TSMU COLLECTION OF SCIENTIFIC WORKS 49 (November 6, 2019): 141–43. http://dx.doi.org/10.52340/csw.v49i0.210.

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The paper presents the modern data concerning the spectrum of electromagnetic radiation and its impact on the structure and function of the skin at various dermatoses. The possibilities of non-drug treatment of dermatoses using different UV spectrum are described. Particular attention is paid to the study of the most effective and safe method for treatment by means of narrow-wave phototherapy with a maximum emission at a wavelength of 311 nm (UVB - 311). The results of the comparative analysis of efficacy and safety of PUVA photochemotherapy and phototherapy UVB -311, on examples of some specific nosologic units (psoriasis, parapsoriasis, vitiligo, mycosis fungoides, photodermatosis, atopic dermatitis) are presented. Based on analysed data, authors conclude that UVB -311 nm is an effective, well-tolerated, safe and alternative method for treatment of chronic dermatoses. The brief review of the available in literature data, allow authors to make conclusion about the possibility of widespread implementation of phototherapy method in practical dermatology.

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39

Patil, Chetan C., Anuj Bhatnagar, Ravishekar N. Hiremath, Debdeep Mitra, Sunmeet Sandhu, and Satish Chand. "Photodermatosis and high UV index in Jorhat (north east India) due to single time zone: A study." Photodermatology, Photoimmunology & Photomedicine 38, no. 2 (October 7, 2021): 178–80. http://dx.doi.org/10.1111/phpp.12733.

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40

Berny-Moreno, Joanna, and Jacek C. Szepietowski. "Neuropathic itch caused by nerve root compression: brachioradial pruritus and notalgia paresthetica / Neuropatski pruritus (svrab) prouzrokovan kompresijom nervnih korenova - brahioradijalni pruritus i nostalgija parestetika." Serbian Journal of Dermatology and Venerology 1, no. 2 (May 1, 2009): 68–72. http://dx.doi.org/10.2478/v10249-011-0006-z.

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Abstract Neuropathic itch (itching or pruritus) arises from a pathology located at any point along the afferent pathway of the nervous system. It may be related to damage to the peripheral nervous system, such as in postherpetic neuropathy, brachioradial pruritus or notalgia paresthetica. It has many clinical features similar to neuropathic pain. Patients complain of itching, which is associated with burning sensation, aching, and stinging. Brachioradial pruritis (BP) is an intense itching sensation of the arm, usually between the shoulder and elbow of one or both arms. It is an enigmatic condition with a controversial etiology; some authors consider BP to be a photodermatosis, whereas other authors attribute BP to compression of cervical nerve roots. Notalgia paresthetica is an isolated mononeuropathy involving the skin over or near the scapula. Patients have a pruritus on the mid-upper back. The treatment is usually difficult, but capsaicin and local analgesic agents are the options of choice. Brachioradial pruritus and notalgia paresthetica are often unrecognized neurocutaneous conditions and therefore, a thorough history and physical examination are of utmost importance to distinguish symptoms and apply accurate therapeutic options.

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41

Yamamoto, M., S. Aochi, C. Suzuki, S. Nakamura, R. Murakami, Y. Ogawa, and H. Takahashi. "A case with good response to belimumab for lupus nephritis complicated by IgG4-related disease." Lupus 28, no. 6 (March 27, 2019): 786–89. http://dx.doi.org/10.1177/0961203319840430.

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Immunoglobulin (Ig)G4-related disease (IgG4-RD) is an unusual complication of systemic lupus erythematosus (SLE). We report a case in which belimumab proved efficacious for not only SLE, but also IgG4-RD. A 58-year-old Japanese woman had suffered from photodermatosis and erythema on the limbs for 20 years. She presented in slight fever and fatigue since 2016. Laboratory data showed hypergammaglobulinemia, proteinuria and positive results for anti-nuclear antibody and anti-double-stranded DNA antibody. Furthermore, elevated levels of serum IgG4 were detected. Contrast-enhanced computed tomography disclosed multiple areas of poor enhancement in the kidneys. The patient was diagnosed with lupus nephritis and IgG4-RD from renal biopsy. Treatment was started with prednisolone at 40 mg/day and mycophenolate mofetil. Proteinuria and serological findings improved initially, but tapering the dose of glucocorticoid proved difficult. After treatment was started with belimumab, clinical symptoms and proteinuria resolved completely. The dose of glucocorticoid was successfully tapered and serum concentration of IgG4 fell further. This appears to represent the first report of a case in which both SLE and IgG4-RD were effectively treated using belimumab.

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42

De Martinis, Massimo, Maria Maddalena Sirufo, and Lia Ginaldi. "Solar urticaria, a disease with many dark sides: is omalizumab the right therapeutic response? Reflections from a clinical case report." Open Medicine 14, no. 1 (June 7, 2019): 403–6. http://dx.doi.org/10.1515/med-2019-0042.

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AbstractSolar urticaria is a rare type of photodermatosis that significantly reduces the quality of life of the subjects affected, with a risk of anaphylaxis should the entire body be exposed to the sun. Patients are forced to modify and limit their normal activities, and since the symptoms are triggered by exposure to sun, which is difficult if not impossible to avoid in everyday life, a safe and effective therapy appears to be essential.Unfortunately, traditional therapies in a discrete number of patients are unable to provide adequate and safe answers.We describe the case of an 18-year-old woman who began to manifest the first symptoms walking under the spring sunshine. A few minutes after sun exposure, itching and burning sensation began, followed immediately by erythema appearance in the photoexposed skin areas.She was treated with non-sedating H1-blocking antihistamines and leukotriene antagonist with no success, so we decided to treat with omalizumab.The satisfactory response after the failure of previous standard therapeutic strategies, confirms the effectiveness of this molecule in the treatment of solar urticaria, which despite what reported in several studies, has not yet been recognized and authorized by the competent Health Authorities in the treatment of this condition.

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Chong, Wei-Sheng, and Shih-Wee Khoo. "Solar urticaria in Singapore: an uncommon photodermatosis seen in a tertiary dermatology center over a 10-year period." Photodermatology, Photoimmunology and Photomedicine 20, no. 2 (April 2004): 101–4. http://dx.doi.org/10.1111/j.1600-0781.2004.00083.x.

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Welti, Michèle, Egle Ramelyte, Reinhard Dummer, and Laurence Imhof. "Evaluation of the minimal erythema dose for UVB and UVA in context of skin phototype and nature of photodermatosis." Photodermatology, Photoimmunology & Photomedicine 36, no. 3 (February 19, 2020): 200–207. http://dx.doi.org/10.1111/phpp.12537.

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Pavanelli, Giovana Memari, Sibele Sauzem Milano, Gabriela Sevignani, Juliana Elizabeth Jung, Vaneuza Araujo Moreira Funke, and Marcelo Mazza do Nascimento. "Furosemide-induced pseudoporphyria in a patient with chronic kidney disease: case report." Brazilian Journal of Nephrology 40, no. 3 (July 10, 2018): 287–90. http://dx.doi.org/10.1590/2175-8239-jbn-2017-0029.

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ABSTRACT Introduction: Pseudoporphyria is a rare photodermatosis with characteristics similar to those of porphyria cutanea tarda, without, however, presenting abnormalities in porphyrin metabolism. Its etiology is related to chronic kidney disease, ultraviolet radiation and certain medications. The aim of the present study is to describe a case of furosemide-related pseudoporphyria in a patient with chronic kidney disease. Case description: A 76-year-old male patient with stage 4 chronic kidney disease and in continuous use of furosemide presented ulcerated lesions with peripheral erythema and central hematic crust in the legs. On a skin infection suspicion, treatment with quinolone and neomycin sulfate was initiated, without improvement. A biopsy of the lesion was performed, with histopathological examination demonstrating findings compatible with porphyria, although the patient did not present high porphyrin levels. The diagnosis of furosemide-induced pseudoporphyria was then established, with medication suspension, and there was a significant improvement of the lesions. Discussion: There are few cases of pseudoporphyria described, but it is believed that this condition is underdiagnosed, especially in patients with chronic kidney disease. Both clinical and histopathological findings closely resemble porphyria, differentiating it from normal levels of porphyrin in plasma, urine, or feces. Conclusions: Although the lesions are mostly benign, they may increase the morbidity and mortality of these patients, so a proper diagnosis and early treatment are extremely important.

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Policarová, Marie. "Photodermatoses." Dermatologie pro praxi 10, no. 2 (July 1, 2016): 60–61. http://dx.doi.org/10.36290/der.2016.014.

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Lim, Henry W., Rudolf L. Baer, and R. William Gange. "Photodermatoses." Journal of the American Academy of Dermatology 17, no. 2 (August 1987): 293–99. http://dx.doi.org/10.1016/s0190-9622(87)80317-1.

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Beani, J. C. "Photodermatoses." EMC - Dermatologie 3, no. 2 (January 2008): 1–31. http://dx.doi.org/10.1016/s0246-0319(08)48447-9.

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Ledo, Elena. "Photodermatoses." Dermatologic Clinics 12, no. 4 (October 1994): 797–803. http://dx.doi.org/10.1016/s0733-8635(18)30143-8.

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Wolf, Ronni, and Oumeish Youssef Oumeish. "Photodermatoses." Clinics in Dermatology 16, no. 1 (January 1998): 41–57. http://dx.doi.org/10.1016/s0738-081x(97)00169-7.

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