Özet
Primer splenik anjiyosarkom, dalak damar endotelinden köken alan, nadir ve agresif bir malign tümördür. Karın ağrısı veya splenomegali ile ortaya çıkabilir; tümör içi kanama ve spontan rüptür hemoperitoneuma ve dolaşım bozulmasına yol açabilir. Kontrastlı BT kitle morfolojisini, kanamayı ve uzak yayılımı birlikte değerlendirir. Görüntüleme özellikleri özgül olmadığından heterojen vasküler kitle anjiyosarkomu düşündürebilir ancak tanı histopatolojiyle doğrulanır.
Faz ve pencere
- Kontrastsız
- Tümör içinde taze kanama varsa çevre parankimden daha yüksek atenüasyonlu odaklar; rüptürde perisplenik ve intraperitoneal yüksek atenüasyonlu kan görülebilir.
- Arteriyel
- Vasküler tümör bileşenleri yamalı veya heterojen kontrastlanabilir; taze kanama genellikle kontrastsız kesitte hiperdens olarak izlenir.
- Portal
- Portal venöz fazda sınırları belirsiz, heterojen kitle izlenir; tümör dokusu ile düşük yoğunluklu alanlar arasında kontrastlanma farkı belirginleşir. Karaciğer ve diğer organlardaki sekonder odaklar evreleme açısından aranır.
Önerilen pencereler: Batın (G 400 / M 50), Karaciğer (G 150 / M 30), Anjiyo (G 600 / M 150).
BT bulguları
- Dalak boyutunu artıran, parankimi yer yer değiştiren veya çok odaklı heterojen solid kitle.
- Kitle içinde nekroz, kistik görünümlü dejenerasyon ve kanama alanları; atenüasyon kontrastsız seride daha belirgin olabilir.
- Kontrastlanma homojen değildir; canlı tümör bileşenleri ile nekrotik bölgeler aynı lezyonda yan yana bulunur.
- Kapsül bütünlüğü kaybı ve perisplenik hematom rüptürü düşündürür.
- Dalak ve karaciğer çevresinde yüksek dansiteli serbest sıvı izlenmesi hemoperitoneumu düşündürür.
- Karaciğer metastazları sık görülen uzak yayılım örüntüsüdür; akciğer, kemik, lenf nodu ve diğer organlar da taranır.
Normalde
Anjiyosarkomda normal splenik parankim diffüz biçimde tümörle yer değiştirebilir; BT'de heterojen kitle ve nekrotik alanları bu parankimle karşılaştır. Dalak boyutundaki artışı ve parankimin tümörle diffüz yer değiştirmesini değerlendir.
Normal BT ile kıyasla
Aynı bölgenin, kaynak veri setinde patoloji içermediği belirtilen bir BT incelemesini kesit kesit kaydırın; organ sınırlarını açarak anatomiyi hasta görüntüsüyle karşılaştırın. Küçük rastlantısal bulgular tümüyle dışlanmamıştır.
Kaynak: TotalSegmentator v2.01 veri seti (Wasserthal ve ark., Radiology: Artificial Intelligence 2023), CC BY 4.0, vaka s0541; organ sınırları veri setinin otomatik segmentasyonundan, birleştirilerek sadeleştirildi. Görüntüler 2,5 mm kesit aralığına yeniden örneklendi.
Ayırıcı tanı
- Splenik lenfoma
- primer dalak maligniteleri arasında en sık görülen gruptur ve genellikle diffüz splenomegali ile seyrederek odaklardan ziyade organ büyümesine yol açar.
- Metastaz
- bilinen primer tümör ve diğer organlarda benzer lezyonlar tanıyı destekler.
- Splenik hemanjiyom
- vasküler yapısı nedeniyle anjiyosarkomla görüntüleme özellikleri açısından örtüşebilir; tanı kesinleştirilemeyince histopatoloji gerektirir.
- Splenik hamartom
- nadir görülen benign bir lezyondur; bulgu ve semptomları genellikle non-spesifik olup, hipersplenizm bulguları eşlik edebilir.
- Enfarkt
- kapsüle tabanı uzanan kama biçimli hipoperfüze alan kitle benzeri tümör dokusundan ayrılır.
Tuzaklar
- Kontrastsız kesitte tümör içi kanama, solid bileşenden ayrılmayabilir; aynı düzeyin kontrastlı serisiyle eşleştir.
- Tümör rüptürüne bağlı taze kanama alanları, kontrastsız BT kesitlerinde hiperatenuasyon olarak belirginleşir.
- Anjiyosarkomda heterojen kontrastlanma görülebileceğinden, bu görünümü tek başına tanı koydurucu kabul etme.
- Karaciğerdeki hipervasküler odakları bağımsız benign lezyon kabul etmeden önce dalak tümörü bağlamında metastaz açısından karşılaştır.
- Dalaktaki heterojen vasküler kitle görüntüleme ile anjiyosarkom olarak kesinleştirilemez; kanama ve yayılımı değerlendir, özgül tümör tanısını histopatolojiye bırak.
Kendini dene
Splenomegalik hastada heterojen, nekroz ve kanama içeren splenik kitle var. Bu özgül olmayan BT görünümünde hangi nadir agresif vasküler tümör ayırıcı tanıda akılda tutulmalıdır?
Cevabı göster
Primer splenik anjiyosarkom. Primer splenik anjiyosarkom heterojen kitle, nekroz ve kanama ile görülebilir; ancak BT görünümü özgül değildir ve hemanjiyom, lenfoma gibi lezyonlarla örtüşür. Görüntüleme tümör şüphesini yükseltir, kesin tanıyı histopatoloji koyar.
Dalak kitlesi çevresinde kanama şüphesi olan hastada kontrastsız BT'de hiperatenuasyon ve intraperitoneal kanama bulguları izleniyor. Bu bulgular neyi düşündürür?
Cevabı göster
Aktif kanama. Kontrastsız BT'de kanamaya bağlı hiperatenuasyon ve yoğun intraperitoneal sıvı, dalak rüptürüne bağlı kanamayı düşündürür.
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Kaynaklar
Bu sayfadaki 38 cümle ve 2 quiz sorusu aşağıdaki kaynaklardan alıntılarla tek tek karşılaştırıldı; 14 cümle bu karşılaştırmada düzeltildi (2026-10-09).
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Eğitim amaçlıdır; hasta başında tanı ve tedavi kararının yerine geçmez. İçerik yapay zekâ destekli bir süreçle güncel literatüre göre cümle cümle kaynaklarla karşılaştırıldı, ancak uzman radyolog incelemesinden geçmedi. Klinik kararlarda güncel kılavuzları, kurum protokollerini ve radyoloji raporunu esas alın.