Journal of Surgical Pathology, we would like to share a case that most likely falls within the
remit of this entity. We described a so-called “plasma cell-rich lymphangiosarcoma” in a 79 …

We have read the interesting article of Scarabello et al. 5 about cutaneous lymphomas with
prominent granulomatous reaction. One of the cases corresponded to a secondary …

Herein, we report a case of cutaneous angiosarcoma in a 35-year-old, morbidly obese
woman. The tumor arose in the most dependent portion of the lower abdominal panniculus …

To the Editor, The course of an angioimmunoblastic T-cell lymphoma (AITL) is diverse, but
overall, it is aggressive and has a poor prognosis. 1 Serous effusions, including pleural …

We read with interest the articles by Arber et al. and Falk et al. in earlier issues of the journal.
1, 3 Recently we encountered an example of a small solitary littoral cell angioma in a 53 …

278 International Journal of Surgical Pathology 27 (3) epithelioid angiosarcoma (Figure 2).
Angiosarcomas are very rare tumors of the gastrointestinal (GI) tract. 6 The clinical …

We recently described a case of splenic littoral cell angiosarcoma (LCAS), a newly
recognized neoplasm thought to show sinus lining cell differentiation (4). Because splenic …

Dear Dr. Bedrossian: Angiosarcomas are malignant tumors that recapitulate many of the
functional and morphologic features of normal endothelium. They are also one of the rarest …

To the Editor: We have read the article by Slack et al 1 with interest. The authors described 3
cases of splenic masses in children; the histology was characterized by “abundant …

Sir, Angioimmunoblastic T-cell lymphoma (AITL) is classified in the revised fourth edition of
the World Health Organization (WHO) classification under nodal T-cell lymphomas with T …