scispace - formally typeset
Open AccessJournal ArticleDOI

Follow‐up study of thymomas with special reference to their clinical stages

TLDR
Seven of 13 patients treated by subtotal resection survived more than five years with postopertive radiotherapy, and the five‐year survival rates of each clinical stage were 92.6% in Stage I, 85.7% in stages II and III, and 50% in stage IV.
Abstract
Follow-up data were obtained for 96 cases of thymoma. The one-year survival rate was 84.3%, the three-year 77.1%, the five-year 74.1%, and the ten-year 57.1%. The five-year survival rate of total resection group was 88.9%; that of non-radically treated group was 44.4%. Clinical stages were defined: Stage I--macroscopically encapsulated and microscopically no capsular invasion; Stage II--1. macroscopic invasion into surrounding fatty tissue of mediastinal pleura, or 2. microscopic invasion into capsule; Stage III--macroscopic invasion into neighboring organ; Stage IVa--pleural or pericardial dissemination; Stage IVb--lymphogenous or hematogenous metastasis. Five-year survival rates of each clinical stage were 92.6% in Stage I, 85.7% in Stage II, 69.6% in Stage III, and 50% in Stage IV. Recurrence after total resection was found in six of 69 cases. Seven of 13 patients treated by subtotal resection survived more than five years with postoperative radiotherapy.

read more

Citations
More filters
Book

Pathology and genetics of tumours of the lung , pleura, thymus and heart

TL;DR: This book will not become a unity of the way for you to get amazing benefits at all, but, it will serve something that will let you get the best time and moment to spend for reading the book.
Journal ArticleDOI

Therapy for thymic epithelial tumors: a clinical study of 1,320 patients from Japan

TL;DR: There is value in debulking surgery in invasive thymoma, but not in thymic carcinoma, and it is doubt that adjuvant therapy is valuable for patients with totally resected invasiveThymic epithelial tumors.
Journal ArticleDOI

The World Health Organization histologic classification system reflects the oncologic behavior of thymoma: a clinical study of 273 patients.

TL;DR: The authors previously reported that the WHO histologic classification system reflects invasiveness and immunologic function of thymic epithelial tumors, and examined the prognostic significance of this classification system.
Journal ArticleDOI

Thymoma. A clinicopathologic review.

TL;DR: The clinical and pathologic features of 283 patients with thymoma treated at the Mayo Clinic were examined and poor prognostic factors included presence of tumor‐related symptoms, large tumor size, local invasion or metastasis in initial operation, and predominantly epithelial histologic features.
References
More filters
Journal ArticleDOI

Thymoma. A clinical and pathological study of 65 cases

TL;DR: A clinicopathologic study of 65 patients with thymomas found that syndromes, particularly myasthenia gravis and red cell hypoplasia, affected survival to an equal or greater extent than did the direct effects of the tumors.
Book

Tumors of the thymus

Journal ArticleDOI

Thymomas: Clinicopathologic features, therapy, and prognosis

TL;DR: Clinopathologic features indicating a poor prognosis were a non‐encapsulated tumor of a predominantly epithelial cell type, superior vena caval syndrome, malignant pleural effusion, supraclavicular lymph node involvement, dysphagia, hoarseness, myasthenia gravis, erythroid hypoplasia, and hypogammaglobulinemia.
Related Papers (5)