𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Schwannoma with angiosarcoma : Report of a case and comparison with other types of nerve tumors with angiosarcoma

✍ Scribed by Ralph I. Rückert; Barbara Fleige; Patrik Rogalla; James M. Woodruff

Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
985 KB
Volume
89
Category
Article
ISSN
0008-543X

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Fine-needle aspiration biopsy of hepatic
Fine-needle aspiration biopsy of hepatic angiosarcoma: Report of a case with immunocytochemical findings
✍ John W. Wong; Dr. Yvan C. Bedard 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 437 KB 👁 1 views

## Abstract Hepatic angiosarcoma (Kupffer cell sarcoma) is a very rare but ominous malignancy. We report a case diagnosed by fine‐needle aspiration biopsy (FNAB). The smear showed malignant spindle cells and a few rounded cells. The diagnosis was made on the cell block by the characteristic scaffol

Epithelioid angiosarcoma of the adrenal
Epithelioid angiosarcoma of the adrenal gland with cytokeratin expression report of a case with accompanying mesenteric fibromatosis
✍ Ofer Ben-Izhak; Lya Auslander; Suzana Rabinson; Chaim Lichtig; Ahud Sternberg 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 767 KB

A case report of epithelioid adrenal angiosarcoma is presented. Tumor cells showed expression of cytokeratin, Factor VIII-related antigen, Ulex europaeus agglutinin-I, and vimentin. The patient also was found to have mesenteric fibromatosis (abdominal desmoid tumor) and an elevated serum level of es

Primary angiosarcoma of the thyroid glan
Primary angiosarcoma of the thyroid gland with recurrence diagnosed by fine needle aspiration: A case report
✍ Nurismah Md. Isa; Daniel T. James; Teong H. Saw; Robert Pennisi; Ian Gough 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 269 KB 👁 2 views

## Abstract Angiosarcoma of the thyroid is a rare and aggressive primary malignant tumor of the thyroid originally reported in patients from the Swiss Alpine region. Diagnosis of this tumor rests mainly on characteristic histopathological features of a malignant vascular tumor supported by immunopo