Isolated Radial Nerve Palsy Due to Metastasis from a Primary Malignant Lymphoma of the Brain

Abstract A malignant lymphoma of the reticulum cell sarcoma variety developed in the right radial nerve of a 60-year-old man 3 years after he had presented with a primary malignant lymphoma of the brain. Serial evaluations and metastatic workups over several years failed to demonstrate evidence of extraneural metastasis.

Download Full-text

Isolated radial nerve palsy due to metastasis from a primary malignant lymphoma of the brain

Neurosurgery ◽

10.1097/00006123-198712000-00020 ◽

1987 ◽

Vol 21 (6) ◽

pp. 905???9 ◽

Cited By ~ 1

Author(s):

V vanBolden ◽

D G Kline ◽

C A Garcia ◽

G D vanBolden

Keyword(s):

Malignant Lymphoma ◽

Radial Nerve ◽

Nerve Palsy ◽

Radial Nerve Palsy ◽

The Brain

Download Full-text

Primary Bioccipital Reticulum Cell Sarcoma: A Case Report with Emphasis on Carbon Dioxide Laser Applicatio

Neurosurgery ◽

10.1227/00006123-198304000-00020 ◽

1983 ◽

Vol 12 (4) ◽

pp. 472-476 ◽

Cited By ~ 1

Author(s):

Mehdi Habibi ◽

Ronald A. Bernstein ◽

James Stone ◽

John Oldershaw ◽

Hwaja L. Rhee

Keyword(s):

Co2 Laser ◽

Carbon Dioxide Laser ◽

Malignant Tumors ◽

Reticulum Cell ◽

Reticulum Cell Sarcoma ◽

Cell Sarcoma ◽

The Right ◽

The Brain ◽

Co2 Laser Ablation

Abstract A case of bilateral occipital primary reticulum cell sarcoma of the brain is reported, and the literature concerning this rare and often confusing tumor is reviewed. Gross total CO2 laser ablation of this infiltrating tumor of the right visual cortex is compared to conventional excision of the left occipital tumor in the same patient. The uniqueness of this case and the role of the CO2 laser in the total excision of such malignant tumors are emphasized.

Download Full-text

Primary Malignant Lymphoma of the Testis: Two Cases of Reticulum Cell Sarcoma

The Journal of Urology ◽

10.1016/s0022-5347(17)65922-6 ◽

1959 ◽

Vol 82 (4) ◽

pp. 504-507 ◽

Cited By ~ 16

Author(s):

Brodie C. Nalle ◽

Emily M. Gray

Keyword(s):

Malignant Lymphoma ◽

Reticulum Cell ◽

Reticulum Cell Sarcoma ◽

Cell Sarcoma

Download Full-text

Primary Reticulum Cell Sarcoma of the Brain in Wiskott-Aldrich Syndrome

Archives of Neurology ◽

10.1001/archneur.1977.00500220067012 ◽

1977 ◽

Vol 34 (10) ◽

pp. 633 ◽

Cited By ~ 26

Author(s):

Lawrence M. Model

Keyword(s):

Reticulum Cell ◽

Reticulum Cell Sarcoma ◽

Cell Sarcoma ◽

Wiskott Aldrich Syndrome ◽

The Brain

Download Full-text

Humeral shaft fracture associated with radial nerve palsy -a case report

Journal of Innovations in Applied Pharmaceutical Science (JIAPS) ◽

10.37022/jiaps.v6i3.251 ◽

2021 ◽

pp. 54-55

Author(s):

Rishitha M ◽

Akasha Sindhu M

Keyword(s):

Radial Nerve ◽

Nerve Palsy ◽

Wrist Joint ◽

Shaft Fracture ◽

Humeral Shaft Fracture ◽

Humeral Shaft ◽

Radial Nerve Palsy ◽

Loss Of Function ◽

History Of ◽

The Right

Radial nerve palsy was induced by radial nerve compression, which was often caused by humerus bone fracture. This leads to pain, weakness, or loss of function mostly in the wrist, hand, and fingers. We reported a case of a 24-year-old male patient with complaints of swelling of the right-hand wrist joint and pain during extension and flexion while moving. He had a three-month history of mild displaced humeral shaft fracture from a traffic accident and an intramedullary Ender nailing was performed. He now has been admitted with swelling in his right wrist joint and pain while moving his hand. The case was diagnosed as Radial nerve palsy. Surgery was performed, the proximal and distal ends of the radial nerve were separated at the humeral bone's surface. The radial nerve stumps were enough long to be sutured. Our one-month follow-up shows no complications. The majority cases of radial nerve palsy will resolve within a few weeks after surgery, as our patient did, and the most prominent is patient education.

Download Full-text

Reticulum cell sarcoma of the brain with Wiskott-Aldrich syndrome

PEDIATRICS ◽

10.1542/peds.54.4.455 ◽

1974 ◽

Vol 54 (4) ◽

pp. 455-455

Author(s):

Robert W. Miller

Keyword(s):

Ataxia Telangiectasia ◽

Reticulum Cell ◽

Renal Transplant Recipients ◽

Transplant Recipients ◽

Reticulum Cell Sarcoma ◽

Cell Sarcoma ◽

Wiskott Aldrich Syndrome ◽

Rare Site ◽

Congenital Immunodeficiency ◽

The Brain

Congenital immunodeficiency predisposes patients with Wiskott-Aldrich syndrome to lymphoreticular neoplasia. A 19-year-old boy with the syndrome has recently been reported with reticulum cell sarcoma confined to the brain, a very rare site for this neoplasm (Heidelberger, K. P., and LoGolvan, D. P., Cancer, 33:281-284, 1974). The same rare neoplasm has been observed in 13 renal-transplant recipients on immunosuppressive therapy (Hoover, R. N., and Fraumeni, J. F., Jr., Lancet, II:55, 1973). The patient with Wiskott-Aldrich syndrome and reticulum cell sarcoma of the brain, unlike those with ataxia-telangiectasia and lymphoma, experienced no adverse reaction to radiotherapy or chemotherapy.

Download Full-text