Literature DB >> 27759698

Occlusive Nonvasculitic Vasculopathy.

Mar Llamas-Velasco1, Victoria Alegría, Ángel Santos-Briz, Lorenzo Cerroni, Heinz Kutzner, Luis Requena.   

Abstract

We review the most characteristic clinical and histopathologic findings of the cutaneous manifestations of the occlusive nonvasculitic vasculopathic disorders. Clinically, most of these conditions are characterized by retiform purpura. Histopathologic findings consist of occlusion of the vessel lumina with no vasculitis. Different disorders may produce nonvasculitic occlusive vasculopathy in cutaneous blood and lymphatic vessels, including embolization due to cholesterol and oxalate emboli, cutaneous intravascular metastasis from visceral malignancies, atrial myxomas, intravascular angiosarcoma, intralymphatic histiocytosis, intravascular lymphomas, endocarditis, crystal globulin vasculopathy, hypereosinophilic syndrome, and foreign material. Other times, the occlusive disorder is due to platelet pugging, including heparin necrosis, thrombocytosis secondary to myeloproliferative disorders, paroxysmal nocturnal hemoglobinuria, and thrombotic thrombocytopenic purpura. Occlusive vasculopathy may also appear in cold-related gelling agglutination, like that occurring in cryofibrinogenemia, cryoglobulinemia, cold agglutinin syndrome, and crystalglobulinemia. Microorganisms may also occlude the vessels lumina and this is especially frequent in ecthyma gangrenosum, opportunistic fungi as aspergillosis or fusariosis, Lucio phenomenon of lepromatous leprosy and disseminated strongyloidiasis. Systemic coagulopathies due to defects of C and S proteins, coumarin/warfarin-induced skin necrosis, disseminated intravascular coagulation, and antiphospholipid antibody/lupus anticoagulant syndrome may also result in occlusive nonvasculitic vasculopathy. Finally, vascular coagulopathies such as Sneddon syndrome, livedoid vasculopathy, and atrophic papulosis may also cause occlusion of the vessels of the dermis and/or subcutis. Histopathologic study of occlusive vasculopathic lesions is the first step to achieve an accurate diagnosis, and they should be correlated with clinical history, physical examination, and laboratory findings to reach a final diagnosis.

Entities:  

Mesh:

Year:  2017        PMID: 27759698     DOI: 10.1097/DAD.0000000000000766

Source DB:  PubMed          Journal:  Am J Dermatopathol        ISSN: 0193-1091            Impact factor:   1.533


  13 in total

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Authors:  Tyson Hawkley; David Chang; Whitney Pollard; David Ferraro
Journal:  BMJ Case Rep       Date:  2017-07-27

2.  An interesting case of small vessel pathology following coronavirus infection.

Authors:  Shadi M Ramadan; Eirini V Kasfiki; Ciaran Wp Kelly; Irshad Ali
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Review 3.  Bar code reader - an algorithmic approach to cutaneous occluding vasculopathies? Part I: small vessel vasculopathies.

Authors:  Gudrun Ratzinger; Bettina G Zelger; Bernhard W Zelger
Journal:  J Dtsch Dermatol Ges       Date:  2019-09-05       Impact factor: 5.584

Review 4.  Bar Code Reader - an algorithmic approach to cutaneous occluding vasculopathies? part II medium vessel vasculopathies.

Authors:  Gudrun Ratzinger; Bettina G Zelger; Bernhard W Zelger
Journal:  J Dtsch Dermatol Ges       Date:  2019-11       Impact factor: 5.584

Review 5.  Ecthyma gangrenosum caused by Staphylococcus aureus in hematological malignancies: Case reports and literature review.

Authors:  Yuka Kudo Nagata; Noritaka Sekiya; Kazuaki Fukushima; Masao Horiuchi; Noriko Doki
Journal:  Medicine (Baltimore)       Date:  2022-08-19       Impact factor: 1.817

6.  Cardiovascular Morbidity in Monoclonal Gammopathy of Undetermined Significance: A Danish Nationwide Study.

Authors:  Brian Schwartz; Morten Schou; Frederick L Ruberg; Dane Rucker; Jihoon Choi; Omar Siddiqi; Kevin Monahan; Lars Køber; Gunnar Gislason; Christian Torp-Pedersen; Charlotte Andersson
Journal:  JACC CardioOncol       Date:  2022-07-19

7.  Retiform purpura as a dermatological sign of coronavirus disease 2019 (COVID-19) coagulopathy.

Authors:  X Bosch-Amate; P Giavedoni; S Podlipnik; C Andreu-Febrer; J Sanz-Beltran; A Garcia-Herrera; L Alós; J M Mascaró
Journal:  J Eur Acad Dermatol Venereol       Date:  2020-06-26       Impact factor: 9.228

8.  Purpura fulminans-like lesions in antiphospholipid syndrome with endothelial C3 deposition.

Authors:  Jorge Magdaleno-Tapial; Cristian Valenzuela-Oñate; Javier Pitarch-Fabregat; María Marín-Jiménez; Clara Molina Almela; Johana Isidora Gutiérrez-Salcedo; Javier Calvo-Catalá; José Luis Sánchez-Carazo; V Alegre-de Miquel
Journal:  JAAD Case Rep       Date:  2018-10-12

9.  A Non-smoking Woman with Anti-phospholipid Antibodies Proved to Have Thromboangiitis Obliterans.

Authors:  Natsuki Shima; Yoichiro Akiyama; Shotaro Yamamoto; Ayako Kokuzawa; Katsuya Nagatani; Masahiro Iwamoto; Daisuke Matsubara; Shigeo Kawai; Kojiro Sato; Seiji Minota
Journal:  Intern Med       Date:  2019-10-07       Impact factor: 1.271

Review 10.  Clinical and Histopathologic Characteristics of the Main Causes of Vascular Occlusion - Part I: Thrombi.

Authors:  M J Beato Merino; A Diago; Á Fernández-Flores; J Fraga; A García Herrera; M Garrido; M Á Idoate Gastearena; M Llamas-Velasco; C Monteagudo; J Onrubia; Y C Pérez-González; N Pérez Muñoz; J J Ríos-Martín; E Ríos-Viñuela; J L Rodríguez Peralto; E Rozas Muñoz; O Sanmartín; C Santonja; Á Santos-Briz; C Saus; J M Suárez Peñaranda; V Velasco Benito
Journal:  Actas Dermosifiliogr (Engl Ed)       Date:  2020-10-09
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