Erişkin Still Hastalığında Belirgin Reaktif Trombositozis
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Tarih
2019
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Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Erişkin still hastalığı (ESH), bilinmeyen nedenlere bağlı gelişen multisistemik inflamatuvar bir hastalıktır. Ateş, artrit ve gövdede tipik olarak görülen somon renklidöküntülerle karakterizedir. Tanı genellikle benzer bulgularla seyreden hastalıkların dışlanmasına ek olarak klinik ve laboratuvar bulgularının birlikteliği ile konur.Lenfadenopati ve lökositoz gibi nonspesifik hematolojik bulgular ve farenjit mevcut olabilir. Reaktif trombositoz ESH’da beklenen bir durumken 1 milyonu geçentrombosit yüksekliği ise nadir görülen bir laboratuvar bulgusudur. Bu olguda erişkin still hastalığına eşlik eden belirgin reaktif trombositoz ve nötrofili ile takip ettiğimiz33 yaşında bir erkek hasta sunulmaktadır. ( Sakarya Tıp Dergisi 2019, 9(2):342-346)
Adult still disease (ASD) is a multi system inflammatory disease of unknown origin. It is an inflammatory disease characterized by fever, arthritis and salmon-colored rash typically seen in the body. The diagnosis is usually made by the association of clinical and laboratory findings in addition to exclusion of diseases with similar findings. Nonspecific hematological findings such as lymphadenopathy and leukocytosis and pharyngitis may be present. Reactive thrombocytosis may be seen but platelet levels exceeding 1 million is a rare laboratory finding. In this case report, we present a 33-year-old male patient who was followed with adult still disease and accompanying reactive thrombocytosis and neutrophilia. ( Sakarya Med J 2019, 9(2):342-346 )
Adult still disease (ASD) is a multi system inflammatory disease of unknown origin. It is an inflammatory disease characterized by fever, arthritis and salmon-colored rash typically seen in the body. The diagnosis is usually made by the association of clinical and laboratory findings in addition to exclusion of diseases with similar findings. Nonspecific hematological findings such as lymphadenopathy and leukocytosis and pharyngitis may be present. Reactive thrombocytosis may be seen but platelet levels exceeding 1 million is a rare laboratory finding. In this case report, we present a 33-year-old male patient who was followed with adult still disease and accompanying reactive thrombocytosis and neutrophilia. ( Sakarya Med J 2019, 9(2):342-346 )
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Sakarya Tıp Dergisi
WoS Q Değeri
Scopus Q Değeri
Cilt
9
Sayı
2
