Results 161 to 170 of about 54,150 (267)

Eccrine Squamous Syringometaplasia Mimicking Acute Cutaneous GVHD in a Pediatric HSCT Recipient: Case Report and Brief Review of the Indexed Literature

Journal of Cutaneous Pathology, Volume 53, Issue 9, Page 792-802, September 2026.
ABSTRACT Eccrine squamous syringometaplasia (ESS) is an uncommon reactive alteration of eccrine ducts, most often reported in oncologic and transplant settings, where it may clinically mimic acute cutaneous graft‐versus‐host disease (GVHD). We describe a 3‐year‐old boy with chronic granulomatous disease who developed a diffuse erythematous eruption 6 ...
Benedetta Galli, Cecilia Catapano, Iacopo Ghini, Mariateresa Rossi, Marina Venturini, Valeria Boccaletti   +5 more
wiley   +1 more source

Genetic and Molecular Dissection of Rhabdomyosarcoma Tumorigenesis

, 2011
Rhabdomyosarcoma is a tumor of skeletal muscle-type histogenesis and the most common pediatric soft tissue cancer. Rhabdomyosarcoma is often caused by one of two chromosomal translocations, t(1;32)(q35;q14) or t(2;13)(p36;q14), that are rhabdomyosarcoma
Edelman, Lauren Alexis
core   +1 more source

Pleomorphic rhabdomyosarcoma of the left lower extremity with synchronous gastric and small intestinal metastases presenting as intussusception: a case report. [PDF]

Front Oncol
Yu R, Chen X.
europepmc   +1 more source

Emerging Techniques in Minimally Invasive Surgery in Hematologic Malignancies

European Journal of Haematology, Volume 117, Issue 3, Page 682-690, September 2026.
ABSTRACT Hematologic malignancies represent the most common cancers in children. While the mainstays of treatment are chemotherapy and potentially hematopoietic stem cell transplant, minimally invasive surgery (MIS) has a role in the diagnosis and management of complications related both to disease and therapy as well as common pediatric surgical ...
Alejandro Chara, Katlyn G. McKay, Harold N. Lovvorn III, Joseph C. Fusco   +3 more
wiley   +1 more source

Oral Embryonal Rhabdomyosarcoma and Its Management: A Rare Enigmatic Pediatric Case Report with Immunohistochemistry. [PDF]

Int J Clin Pediatr Dent
Augustine D, Sowmya SV, Rajaram RB, Prasad K, Mondal K, Palanivelu H.   +5 more
europepmc   +1 more source

Advances and Challenges in the Multidisciplinary Treatment of Retroperitoneal Infantile Fibrosarcoma in Early Life

European Journal of Haematology, Volume 117, Issue 3, Page 548-555, September 2026.
ABSTRACT Background and Aims Retroperitoneal Infantile Fibrosarcoma (RIFS) is a rare, locally aggressive pediatric soft tissue tumor. Its retroperitoneal location poses challenges due to proximity and potential invasion of critical structures such as the inferior vena cava (IVC).
Gaia Brunetti, Angelo Zarfati, Giorgio Persano, Giuseppe Maria Milano, Ida Russo, Gian Luigi Natali, Rita Alaggio, Alessandro Crocoli, Chiara Grimaldi   +8 more
wiley   +1 more source

Molecular genetics of childhood rhabdomyosarcoma

, 1989
Rhabdomyosarcoma is a class of malignant neoplasms composed of cells histologically resembling fetal striated muscle. It is the most common soft tissue tumor of children, adolescents, and young adults.
Scrable, Heidi
core  

A Spinal Cord Sarcoma With EWSR1::WT1 Fusion Exhibited Ewing Sarcoma‐Like Pattern Rather Than Desmoplastic Small Round Cell Tumor

Pathology International, Volume 76, Issue 9, September 2026.
We received a case of a 22 years old female, with a spinal cord sarcoma. The tumor consisted of small blue round cells, lack of desmoplastic stroma, with positive expression of CD99 and Desmin in IHC, negative expression of NKX2.2 in IHC, separative signals of EWSR1 gene probe in FISH, gene fusion of EWSR1(E9)::WT1(E8) through RNA and DNA NGS.
Chuqian Zeng, Yishan Wang
wiley   +1 more source

Rhabdomyosarcoma Metastatic to Bone Marrow

, 2002
rhabdomyosarcoma metastatic to bone ...
Lawrence, Christine
core  

TANC1::HTRA1 fusion in schwannomas

Brain Pathology, Volume 36, Issue 5, September 2026.
Ilay Caliskan, Kanish Mirchia, Walter Patrick Devine, Melike Pekmezci   +3 more
wiley   +1 more source