Results 21 to 30 of about 259,450 (135)

Perivascular epithelioid cell tumor of the lung: A case report and literature review

Thoracic Cancer, Volume 13, Issue 17, Page 2542-2553, September 2022., 2022
In this work, we reported a rare case of perivascularepithelioid cell tumor (PEComa) of the lung, and also conducted a systematicliterature review and discussion. The overall efficacy of the patient wasevaluated as stable disease (SD) after systemic therapy, and the patient'scondition was stable during continuous outpatient follow‐up.
Shaofu Yu, Shasha Zhai, Qian Gong, Xiaoping Hu, Wenjuan Yang, Liyu Liu, Yi Kong, Lin Wu, Xingxiang Pu   +8 more
wiley   +1 more source

Pleomorphic liposarcoma with liver metastasis diagnosed by combined fine‐needle aspiration cytology and core‐needle biopsy

Diagnostic Cytopathology, Volume 50, Issue 1, Page E28-E31, January 2022., 2022
Abstract Pleomorphic liposarcoma (PLPS) is the rarest liposarcoma subtype, with high‐local recurrence and metastasis rates. Fine‐needle aspiration cytology (FNAC) is successfully used in the diagnosis of primary or metastatic soft tissue tumors, but liver metastases of PLPS diagnosed by FNAC have never been reported.
Valeria Ciliberti, Pasquale Cretella, Pio Zeppa, Alessandro Caputo   +3 more
wiley   +1 more source

Resection of Primary Renal Leiomyosarcoma Involving the Inferior Vena Cava (IVC) with IVC Resection and Reconstruction

Case Reports in Surgery, Volume 2022, Issue 1, 2022., 2022
Renal leiomyosarcoma is a rare, aggressive tumor of the smooth muscles of the kidney. In our case, the tumor has special characteristics that made it highly challenging, as it involved major vessels and other adjacent vital structures. The rarity of the tumor type itself and the special challenging features we faced intraoperatively encouraged us to ...
Khaled Alshawwa, Jamal Hijazi, Bashar Jaber, Haitham AlHassan, Thaer Abu-Amer, Riyad Salahaldeen, Omar Abu-Zaydeh, Riad Haddad, Christophoros Foroulis   +8 more
wiley   +1 more source

Cancer registry study of malignant hepatic vascular tumors: hepatic angiosarcomas and hepatic epithelioid hemangioendotheliomas

Cancer Medicine, Volume 10, Issue 24, Page 8883-8890, December 2021., 2021
In the current manuscript, we performed a retrospective analysis using the Surveillance, Epidemiology, and End Results Registry (SEER) database to have the most updated characterization of the two most prevalent histological malignant hepatic vascular tumors; angiosarcomas and epithelioid hemangioendotheliomas.
Constanza Martínez, Jonathan K. Lai, Daryl Ramai, Antonio Facciorusso, Zu‐Hua Gao   +4 more
wiley   +1 more source

Primary hepatic perivascular epithelioid cell tumor: A case report and review of literature

Human Pathology Reports, 2023
Primary hepatic perivascular epithelioid cell tumors (PEComas) are extremely rare soft-tissue tumors with few published reports. Herein, a case of a primary hepatic PEComa is reported, along with a review of relevant literature.
Komson Wannasai, Puwitch Charoenchue, Worakitti Lapisatepun, Tarathep Wongsuriyathai, Sarawut Kongkarnka   +4 more
doaj   +1 more source

Ectopic pregnancy of the fundal myometrium in a patient with tuberous sclerosis

Clinical Case Reports, Volume 9, Issue 7, July 2021., 2021
A myometrial ectopic pregnancy is a rare and potentially fatal diagnosis. This diagnosis should be considered when presented with large increases in serum beta‐hCG with no evidence of an intrauterine pregnancy, particularly with altered myometrium. Abstract A myometrial ectopic pregnancy is a rare and potentially fatal diagnosis.
Neha Sharma, Michele Agustin, Ariel Polonsky, Lance Bruck   +3 more
wiley   +1 more source

TFE3 activation in a TSC1‐altered malignant PEComa: challenging the dichotomy of the underlying pathogenic mechanisms

The Journal of Pathology: Clinical Research, Volume 7, Issue 1, Page 3-9, January 2021., 2021
Abstract Perivascular epithelioid cell tumors (PEComas) form a family of rare mesenchymal neoplasms that typically display myomelanocytic differentiation. Upregulation of mTOR signaling due the inactivation of TSC1/2 (Tuberous Sclerosis 1 and 2) is believed to be a key oncogenic driver in this disease.
Maren Schmiester, Anna Dolnik, Uwe Kornak, Berit Pfitzner, Michael Hummel, Denise Treue, Arndt Hartmann, Abbas Agaimy, Veronika Weyerer, Anja Lekaj, Susanne Brakemeier, Robert Peters, Robert Öllinger, Sven Märdian, Lars Bullinger, Jana Käthe Striefler, Anne Flörcken   +16 more
wiley   +1 more source

[Retracted] A Systematic Review of Lymphangioleiomyomatosis on Diagnosis and Molecular Mechanism

BioMed Research International, Volume 2021, Issue 1, 2021., 2021
Objective. Lymphangioleiomyomatosis (LAM) is a rare low‐grade metastatic tumor; however, LAM patients were always found in young age with difficulty for diagnosis. Our study is aimed at observing the clinical characteristics of patients with lymphangiomatosis, including the clinical manifestations, imaging findings, histopathological features, and ...
Xiaotong Dong, Lvcheng Jin, Ailan Wang, Liping Wu, Xintong Fan, Qian Hou, Tianbao Li, Ruilian Zhao, Yunxiang Zhang, Min Tang   +9 more
wiley   +1 more source

Two in One: Epithelioid angiomyolipoma within a classic kidney angiomyolipoma - a case report [PDF]

, 2018
Background Epithelioid angiomyolipoma is defined as potentially malignant mesenchymal neoplasm, characterized by proliferating epithelioid cells, whereas classic angiomyolipoma, composed of fat, smooth muscle cells and dysmorphic vessels, is defined as a
Walter Gysel, Gerd Stuckmann, Jan Tuma, Holger Moch, Andreas L. Serra   +4 more
core   +2 more sources

Renal Epithelioid Angiomyolipoma in Children [PDF]

, 2021
Renal angiomyolipoma is a rare cause of renal tumor in children. Most are associated with tuberous sclerosis, and the classic type is observed more commonly.
Agarwala, Sandeep, Mahajan, Dhruv, Ramteke, Prashant P, Jana, Manisha, Jain, Vishesh   +4 more
core   +1 more source