Exact(12)
Based on morphological and immunohistochemical findings, the tumor was diagnosed as a cutaneous Kaposiform haemangioendothelioma (KHE), a rare, low-grade malignant vascular neoplasm.
The possible causes include hemorrhage from a highly vascular neoplasm, pathological splenic rupture, hemorrhage or rupture of an ovarian cyst, rupture of the gestational sac or other affected anatomic part in an ectopic pregnancy, bleeding from a vascular lesion, anticoagulation therapy, blood dyscrasias, surgery and invasive procedures.
Kaposi's sarcoma (KS) is a multifocal vascular neoplasm that develops in conjunction with HIV infection and AIDS.
Kaposi's sarcoma (KS) is a vascular neoplasm characterized by the dysregulated expression of angiogenic and inflammatory cytokines.
Kaposi's sarcoma (KS) is a multifocal vascular neoplasm invariably associated with infection with the KS-associated human herpesvirus (KSHV/HHV8), which is characterized by cytokine dysregulation [1].
Hemangiopericytoma constitutes <1% of all vascular neoplasm.
Similar(48)
Carotid body tumors (CBT) are rare, infrequently malignant vascular neoplasms that are near the carotid bifurcation.
IL-8-transfected cells produced rapidly growing, highly vascular neoplasms as compared to control cells.
Although anti-NRR antibodies have been developed, sustained treatment with these antibodies will likely cause vascular neoplasms [ 36].
Recent evidence that chronic DLL4 inhibition induces vascular neoplasms [ 23] casts doubt on the safety of this approach.
Juvenile nasopharyngeal angiofibromas (JNA) are histologically benign, slow growing, locally invasive vascular neoplasms that arise from myofibroblasts.
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