𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Diseases of the adolescent female breast a clinico-pathological study

✍ Scribed by A. T. Sandison; J. C. Walker

Publisher
John Wiley and Sons
Year
1968
Tongue
English
Weight
698 KB
Volume
55
Category
Article
ISSN
0007-1323

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Primary and metastatic rhabdomyosarcoma
Primary and metastatic rhabdomyosarcoma in the breast: Neoplasms of adolescent females, a report from the Intergroup Rhabdomyosarcoma Study
✍ Hays, Daniel M.; Donaldson, Sarah S.; Shimada, Hiroyuki; Crist, William M.; Newt πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 150 KB πŸ‘ 2 views

The occurrence of rhabdomyosarcoma (RMS) primary in or metastatic to breast has been regarded as an uncommon event, associated with an unfavorable outcome. Records of 26 patients with diagnoses of breast RMS, either primary or secondary, entered in the Intergroup Rhabdomyosarcoma Study (IRS) (1972-1

Mucinous carcinoma of the breast: A path
Mucinous carcinoma of the breast: A pathologic study of 82 cases
✍ Saudade AndrΓ©; Fernando Cunha; Jorge Soares; MΓ‘rio Bernardo; J. Meneses E Sousa; πŸ“‚ Article πŸ“… 1995 πŸ› John Wiley and Sons 🌐 English βš– 537 KB

## Abstract A series of 82 consecutive cases of mucinous carcinomas of the female breast was investigated for their clinical, morphological, and histochemical features and for the influence of some tumor characteristics on its prognosis. Two groups, a β€œpure” subtype (n=58) and a β€œmixed” subtype (n=

Radiation-induced sarcoma of the breast
Radiation-induced sarcoma of the breast in a female adolescent. Case report with histologic and therapeutic considerations
✍ R. Squire; A. Bianchi; S. M. Jakate πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 477 KB πŸ‘ 2 views

A 14-year-old girl developed a radiation-induced sarcoma of the left breast after successful combined surgical and radiation therapy of a left adrenal carcinoma when she was 9 months old. The breast lesion was histologically described as a stromal sarcoma with fibrosarcomatous and myxosarcomatous ar