3.A Case of Benign Metastasizing Leiomyoma with Multiple Metastasis to the Soft Tissue, Skeletal Muscle, Lung and Breast.
Ji Hoon JO ; Jin Hwa LEE ; Dae Cheol KIM ; Sung Hyun KIM ; Hyuk Chan KWON ; Jae Seok KIM ; Hyo Jin KIM
The Korean Journal of Internal Medicine 2006;21(3):199-201
Benign metastasizing leiomyoma (BML) is composed of well-differentiated smooth muscle cells and dense connective tissue. BML affects middle-aged women who have had previous hysterectomies due to a histologically benign-appearing uterine leiomyoma. We report here on a case of BML from the uterine leiomyoma in a 39-year-old woman that involved the soft tissues, skeletal muscles, lungs and breasts. She underwent a hysterectomy for the uterine leiomyoma, double oophorectomy for hormonal ablation and lung wedge resection to confirm the diagnosis. The microscopic findings of the breast and lung tumor were similar to those of the benign uterine leiomyoma. Therefore, we consider that these lesions were breast and pulmonary metastases of the uterine leiomyoma. We report here on a rare case of benign metastasizing uterine leiomyoma that involved the soft tissue, skeletal muscles, lungs and breasts, and we include a review of the relevant literature.
Uterine Neoplasms/*pathology/surgery
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Tamoxifen/therapeutic use
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Soft Tissue Neoplasms/*secondary
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Muscle, Skeletal/pathology
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Muscle Neoplasms/*secondary
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Lung Neoplasms/*secondary
;
Leiomyoma/drug therapy/*pathology
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Hysterectomy
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Humans
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Female
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Breast Neoplasms/*secondary
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Antineoplastic Agents/therapeutic use
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Adult
4.Synchronous Bony and Soft Tissue Metastases from Follicular Carcinoma of the Thyroid.
Gabriel RODRIGUES ; Arnab GHOSH
Journal of Korean Medical Science 2003;18(6):914-916
Follicular carcinoma of the thyroid rarely manifests itself as a distant metastatic lesion, and, when present, is usually found in flat bones. A soft tissue metastasis is extremely rare, and synchronous metastases to the bone and soft tissue is not reported in the literature so far. We report such a case of a 42-yr-old male, who presented with a goiter, scalp and forearm soft tissue swellings, and, fine needle aspiration cytology of all these swellings revealed a follicular neoplasm. A wide excision of the forearm swelling was carried out and the histopathology was consistent with features of metastatic follicular carcinoma of the thyroid. The main stay of treatment is surgical resection of the primary tumor. The various modalities of treatment of metastasis is discussed with a review of literature.
Adenocarcinoma, Follicular/*pathology/surgery
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Adult
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Bone Neoplasms/pathology/*secondary/surgery
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Human
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Male
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Soft Tissue Neoplasms/pathology/*secondary/surgery
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Thyroid Neoplasms/*pathology/surgery
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Treatment Outcome
6.Metastasis of Transitional Cell Carcinoma to the Lower Abdominal Wall 20 Years after Cystectomy.
Ja Hyeon KU ; Woon Geol YEO ; Min Young PARK ; Eun Sik LEE ; Hyeon Hoe KIM
Yonsei Medical Journal 2005;46(1):181-183
Iatrogenic implantation has been the main cause in the majority of cases of transitional call carcinoma (TCC) with metastasis to the abdominal wall. A 66-year-old woman had undergone radical cystectomy 20 years prior to presenting. Radiological investigations revealed one mass in the left lower abdominal wall and one mass in the right inguinal area. She underwent wide excision of the lesions that revealed metastasis of TCC. This report describes this case of a woman with bladder carcinoma who developed a metastasis in the anterior abdominal wall following an apparent disease-free interval of 20 years.
Abdominal Wall/*pathology
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Aged
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Bladder Neoplasms/*pathology/*surgery
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Carcinoma, Transitional Cell/*secondary/*surgery
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Cystectomy
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Female
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Humans
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Soft Tissue Neoplasms/*secondary
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Time Factors
7.Glomus Tumor of Hoffa's Fat Pad and Its Management by Arthroscopic Excision.
Sharad PRABHAKAR ; Mandeep Singh DHILLON ; Rakesh Kumar VASISHTHA ; Kamal BALI
Clinics in Orthopedic Surgery 2013;5(4):334-337
We present a rare case of glomus tumor of Hoffa's fat pad in a 42-year-old woman. Magnetic resonance imaging findings along with the characteristic clinical picture led us to suspect a glomus tumor as the possible etiology. An ischemia test was found to be positive and this further substantiated our diagnosis. An arthroscopic excision was performed and the histology confirmed the diagnosis of glomus tumor of Hoffa's fat pad. The patient responded well to the excision with immediate complete resolution of pain and she remains asymptomatic at the last follow-up after 15 months. To our knowledge, this is the second reported case of glomus tumor of Hoffa's fat pad and the first ever to be managed by simple arthroscopic excision. The tumor poses a great challenge to an orthopedic surgeon. However, knowledge of its characteristic clinical presentation and the recognition of such a rare entity can help achieve an early diagnosis and timely management.
Adipose Tissue/pathology/*surgery
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Adult
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Arthroscopy
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Female
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Glomus Tumor/*secondary
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Humans
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Knee/pathology/*surgery
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Magnetic Resonance Imaging
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Soft Tissue Neoplasms/*surgery
8.Needle tract seeding following percutaneous biopsy of renal cell carcinoma.
Dwayne T S CHANG ; Hariom SUR ; Mikhail LOZINSKIY ; David M A WALLACE
Korean Journal of Urology 2015;56(9):666-669
A 66-year-old man underwent computed tomography-guided needle biopsy of a suspicious renal mass. Two months later he underwent partial nephrectomy. Histology revealed a 30-mm clear cell renal cell carcinoma, up to Fuhrman grade 3. An area of the capsule was interrupted, which corresponded to a hemorrhagic area on the cortical surface. Under microscopy, this area showed a tongue of tumor tissue protruding through the renal capsule. A tumor deposit was found in the perinephric fat. These features suggest that tumor seeding may have occurred during the needle biopsy.
Adipose Tissue/*pathology
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Aged
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Biopsy, Needle/*adverse effects
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Carcinoma, Renal Cell/*secondary/surgery
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Humans
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Image-Guided Biopsy/adverse effects
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Kidney/*pathology
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Kidney Neoplasms/*pathology/surgery
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Male
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*Neoplasm Seeding
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Soft Tissue Neoplasms/*secondary
9.A Case of Low-grade Fibromyxoid Sarcoma of the Colon.
Min KIM ; Tae Jun SONG ; Seung Dae KANG ; Jong Sik KANG ; Jin Suk KIM ; June Sung LEE ; Chul Nam KIM ; Han Seong KIM
The Korean Journal of Gastroenterology 2014;64(6):375-379
Low-grade fibromyxoid sarcoma is a slowly growing soft tissue neoplasm that shows benign histologic features but may have clinical course of malignant disease. It has been reported to occur in the thigh, inguinal area, axilla, shoulder, neck, perineum or buttock. However, there have been few cases of abdominal organ involvement. A 21-year-old woman presented with a large palpable abdominal mass. A 7x4 cm sized round soft tissue tumor at right upper quadrant area was identified by abdominopelvic CT scan. Percutaneous ultrasound-guided biopsy revealed features of spindle cell tumor. On exploration, the tumor originated from transvers colon and was attached to gastrocolic ligament, transverse mesocolon and stomach. The tumor could be dissected with transverse colectomy and partial gastrectomy. The excised tumor, measuring 7x5x5 cm, was well demarcated and appeared as an ovoid mass with firm and myxoid cut surface. She was diagnosed with low-grade fibromyxoid sarcoma arising from transverse colon, and is currently being followed-up without recurrence or metastasis.
Colon, Transverse
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Female
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Humans
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S100 Proteins/metabolism
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Sarcoma/*diagnosis/pathology/surgery
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Soft Tissue Neoplasms/*diagnosis/pathology/surgery
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Stomach Neoplasms/pathology/secondary
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Tomography, X-Ray Computed
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Young Adult
10.A Case of Alveolar Soft Part Sarcoma of the Pleura.
Hyeong Uk JU ; Kwang Won SEO ; Yangjin JEGAL ; Jong Joon AHN ; Young Jik LEE ; Young Min KIM ; Chulho OAK ; Seung Won RA
Journal of Korean Medical Science 2013;28(2):331-335
Alveolar soft part sarcoma (ASPS) is a rare malignant soft-tissue neoplasm of unknown histogenesis. The two main sites of occurrence are the lower extremities in adults and the head and neck in children. We report the first case of pleural ASPS occurring in a 58-yr-old man who presented with progressive dyspnea. A computed tomographic scan of the thorax revealed a large enhancing pleural mass with pleural effusion in the left hemithorax. Wide excision of the pleural mass was performed. Histologically, the tumor consisted of organoid nests of large polygonal cells, the cytoplasm of which had eosinophilic and D-PAS positive granules. Immunohistochemical staining showed that the tumor cell nuclei were positive for transcription factor 3 (TFE3). The pleural ASPS with multiple bone metastases recurred 1 yr after surgery and the patient died of acute pulmonary embolism 1.5 yr after diagnosis.
Bone Neoplasms/diagnosis/secondary
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Dyspnea/etiology
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Humans
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Immunohistochemistry
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Male
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Middle Aged
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Pleura/physiopathology
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Positron-Emission Tomography and Computed Tomography
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Pulmonary Embolism/diagnosis
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Sarcoma, Alveolar Soft Part/*diagnosis/pathology/radiography
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Soft Tissue Neoplasms/*diagnosis/pathology/radiography
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Transcription Factor 3/metabolism