Bellalah Ahlem, Korbi Ibtissem, Ben Hammouda Seifeddine, Achour Asma, Ben Abdeljelil Nouha, Njima Manel, Daldoul Amira, Hadhri Rim, Njim Leila, Zakhama Abdelfatteh
Department of Pathology, Fattouma Bourguiba University Hospital, Monastir, 5000, Tunisia.
Faculty of Medicine, University of Monastir, Monastir, 5000, Tunisia.
Ann Med Surg (Lond). 2021 Jul 27;68:102638. doi: 10.1016/j.amsu.2021.102638. eCollection 2021 Aug.
Histiocytic sarcoma (HS) is a rare malignant neoplasm showing morphologic and immunohistochemical features of histiocytes. It is characterized typically by extranodal presentation and a poor clinical course, particularly in cases with disseminated disease.
This report documents a case of bifocal and aggressive HS in small bowel and lung revealed by acute peritonitis in a 63-year-old man.
Despite its rarity, we believe that the correct diagnosis of HS is crucial for clinical treatment and prognostic prediction.
The collection of additional cases of HS are important to obtain further progress in prognosis and guide treatment decisions.
组织细胞肉瘤(HS)是一种罕见的恶性肿瘤,具有组织细胞的形态学和免疫组化特征。其典型特征为结外表现和不良的临床病程,尤其是在疾病播散的情况下。
本报告记录了一名63岁男性因急性腹膜炎发现的小肠和肺双灶性侵袭性HS病例。
尽管HS罕见,但我们认为正确诊断对临床治疗和预后预测至关重要。
收集更多HS病例对于在预后方面取得进一步进展和指导治疗决策很重要。