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Found 25 results

  1. Raul Alfredo Borracci

    Pulmonary artery sarcoma resected - stl file processed

    Version 1.0.0

    13 downloads

    Pulmonary artery sarcoma resected - stl file processed Have embodi3D 3D print this model for you. Learn More. This file was created with democratiz3D. Automatically create 3D printable models from CT scans. Learn more. Pulmonary artery sarcoma after surgical resection, bone .stl,chest, thorax, pulmonary, trunk, sarcoma, artery, surgical, resection, heart, ventricle, auricle, clavicle, ribs, dorsal, spine, transverse, spinous, process, sternum,

    Free

  2. Raul Alfredo Borracci

    Pulmonary artery sarcoma resected

    Version 1.0.0

    2 downloads

    Pulmonary artery sarcoma after surgical resection, ct, scan, with, contrast, .stl, axial, dicom, bone, chest, thorax, pulmonary, trunk, sarcoma, artery, surgical, resection, heart, ventricle, auricle, deltoid, pectoris, major, lesser, axillary, carotid, subclavian, trachea, esophagus, bronchi, lung, esophagus, pancreas, small, bowell, ribs, portal, vessels, cava, dorsal, lumbar, spine, transverse, spinous, process

    Free

  3. Raul Alfredo Borracci

    Pulmonary artery sarcoma1

    Version 1.0.0

    8 downloads

    Pulmonary artery sarcoma, ct, with contrast, .stl, axial, dicom, thorax, abdominal, lung, pulmonary, trunk, aorta, arch, ascendent, descendent, sarcoma, heart, ventricle, auricle, septum, muscle, cava, vein, superior, inferior, celiac, mesentery, renal, arteries, kidneys, spleen, liver, pleural effusion, diaphragm, psoas, ribs, bone, scapula, clavicle, subscapularis, supraaortic, portal, veins, trachea, esophagus, stomach, shoulder, small, bowel, colon

    Free

  4. Raul Alfredo Borracci

    Pulmonary sarcoma

    Version 1.0.0

    5 downloads

    Sarcoma, pulmonary artery, thorax, chest, bone, 3d, model, ct, scan, with , contrast , ribs, muscle, pulmonary, trunk, heart, cavities, auricles, ventricles, septum, diaphragm, aorta, ascendent, descendent, arch, subclavian, carotid, clavicle, scapula, lung, liver, portal, vessels, spleen, perisplenic, liquid, dorsal, spine, medulla, canal, muscles, pleura, printable,

    Free

  5. Version 1.0.0

    1 download

    This 3D printable STL file contains a model of the muscles of the left calf and knee was derived from a real medical CT scan. This 60 year old woman has a soft tissue sarcoma involving the left calf muscle (gastrocnemius) which results in a somewhat bulging appearance of this muscle. This model was created using the democratiz3D free online 3D model creation service. STS_010

    Free

  6. Version 1.0.0

    3 downloads

    This 3D model represents a case of high grade leiomyosarcoma implicating the left groin region of a 24 years old female. The patient was treated by surgical excision follower by chemotherapy as well as radiotherapy. A cross sectional CT image is attached showing the lesion in axial, coronal and sagittal planes. Leiomyosarcoma (LMS) is a very rare malignant neoplasm that arises from smooth muscle cells and is considered to be the malignant extension of leiomyoma. Leiomyosarcoma is classified under soft tissue tumours and represents around 8% of all soft tissue malignant tumours. Common locations affected by leiomyosarcoma are: the uterus, retroperitoneum, stomach, oesophagus, small intestine and generally anywhere with smooth muscles. Leiomyosarcoma appears heterogeneous in CT with common central attenuation representing necrosis. This 3D model was created from the file STS_036 The source CT scan used to create this model can be found here.

    Free

  7. Version 1.0.0

    2 downloads

    This model is the bilateral thigh muscle rendering of a 65-year-old male with left thigh myxoid fibrosarcoma. At the time of diagnosis, the patient had metastases to his lungs. The patient therefore underwent neoadjuvant radiotherapy, surgery, and adjuvant chemotherapy and was found to have an intermediate grade lesion at the time of diagnosis. The patient unfortunately died 9.5 months after diagnosis. This is an STL file created from DICOM images of his CT scan which may be used for 3D printing. Myxoid fibrosarcoma (or myxoid MFH) is the most common subtype of MFH, at about 10%-20% of cases. Clinically, the tumor presents as a deep, slow-growing, painless mass. It is located more commonly in the lower extremities and retroperitoneum. Imaging on MRI demonstrates a mass with low signal intensity on T1-weighting imaging, and high signal intensity on T2-weighted imaging. On histology, a myxoid background is present with a storiform (or cartwheel) pattern seen on low-power imaging, seen in fibrosarcomas. A “myxoid background” is composed of a clear, mucoid substance. Treatment includes radiation, wide surgical resection, and chemotherapy in selected cases. However, the 5-year survival is 50%-60% depending on size, grade, depth and presence of metastasis. The term “malignant fibrous histiocytoma” was coined in the 1960s by Margaret R. Murray when histology a sarcoma demonstrated an appearance like histiocytes, with characteristics of phagocytosis and a pleomorphic pattern. With further research, this entity was identified to have a wider range of appearances with a fibrous characteristic. Today, these sarcomas are known as “pleomorphic sarcomas.” Recently, a change in the understanding of soft tissue tumors has purported that MFH is not a specific type of cancer, but a common morphologic pattern shared by unrelated tumors. One school of thought states that this morphologic pattern is shared by tumors as a common final pathway in cancer progression whereas another school of thought believes that true pleomorphic sarcomas are the result of a transformation from mesenchymal stem cells. Future research into understanding the pathway of these sarcomas and progression will help to target specific therapies and, hopefully, eventual cures. This model was created from the file STS_023.

    Free

  8. Version 1.0.0

    6 downloads

    This model is the left thigh muscle rendering of a 65-year-old male with left thigh myxoid fibrosarcoma. At the time of diagnosis, the patient had metastases to his lungs. The patient therefore underwent neoadjuvant radiotherapy, surgery, and adjuvant chemotherapy and was found to have an intermediate grade lesion at the time of diagnosis. The patient unfortunately died 9.5 months after diagnosis. This is an STL file created from DICOM images of his CT scan which may be used for 3D printing. Myxoid fibrosarcoma (or myxoid MFH) is the most common subtype of MFH, at about 10%-20% of cases. Clinically, the tumor presents as a deep, slow-growing, painless mass. It is located more commonly in the lower extremities and retroperitoneum. Imaging on MRI demonstrates a mass with low signal intensity on T1-weighting imaging, and high signal intensity on T2-weighted imaging. On histology, a myxoid background is present with a storiform (or cartwheel) pattern seen on low-power imaging, seen in fibrosarcomas. A “myxoid background” is composed of a clear, mucoid substance. Treatment includes radiation, wide surgical resection, and chemotherapy in selected cases. However, the 5-year survival is 50%-60% depending on size, grade, depth and presence of metastasis. The term “malignant fibrous histiocytoma” was coined in the 1960s by Margaret R. Murray when histology a sarcoma demonstrated an appearance like histiocytes, with characteristics of phagocytosis and a pleomorphic pattern. With further research, this entity was identified to have a wider range of appearances with a fibrous characteristic. Today, these sarcomas are known as “pleomorphic sarcomas.” Recently, a change in the understanding of soft tissue tumors has purported that MFH is not a specific type of cancer, but a common morphologic pattern shared by unrelated tumors. One school of thought states that this morphologic pattern is shared by tumors as a common final pathway in cancer progression whereas another school of thought believes that true pleomorphic sarcomas are the result of a transformation from mesenchymal stem cells. Future research into understanding the pathway of these sarcomas and progression will help to target specific therapies and, hopefully, eventual cures. This model was created from the file STS_023.

    Free

  9. Version 1.0.0

    2 downloads

    This model is the left lower extremity skin rendering of a 65-year-old male with left thigh myxoid fibrosarcoma. At the time of diagnosis, the patient had metastases to his lungs. The patient therefore underwent neoadjuvant radiotherapy, surgery, and adjuvant chemotherapy and was found to have an intermediate grade lesion at the time of diagnosis. The patient is still living with the metastatic disease at 2.5 years since diagnosis. This is an STL file created from DICOM images of his CT scan which may be used for 3D printing. Myxoid fibrosarcoma (or myxoid MFH) is the most common subtype of MFH, at about 10%-20% of cases. Clinically, the tumor presents as a deep, slow-growing, painless mass. It is located more commonly in the lower extremities and retroperitoneum. Imaging on MRI demonstrates a mass with low signal intensity on T1-weighting imaging, and high signal intensity on T2-weighted imaging. On histology, a myxoid background is present with a storiform (or cartwheel) pattern seen on low-power imaging, seen in fibrosarcomas. A “myxoid background” is composed of a clear, mucoid substance. Treatment includes radiation, wide surgical resection, and chemotherapy in selected cases. However, the 5-year survival is 50%-60% depending on size, grade, depth and presence of metastasis. The term “malignant fibrous histiocytoma” was coined in the 1960s by Margaret R. Murray when histology a sarcoma demonstrated an appearance like histiocytes, with characteristics of phagocytosis and a pleomorphic pattern. With further research, this entity was identified to have a wider range of appearances with a fibrous characteristic. Today, these sarcomas are known as “pleomorphic sarcomas.” Recently, a change in the understanding of soft tissue tumors has purported that MFH is not a specific type of cancer, but a common morphologic pattern shared by unrelated tumors. One school of thought states that this morphologic pattern is shared by tumors as a common final pathway in cancer progression whereas another school of thought believes that true pleomorphic sarcomas are the result of a transformation from mesenchymal stem cells. Future research into understanding the pathway of these sarcomas and progression will help to target specific therapies and, hopefully, eventual cures. This model was created from the file STS_022.

    Free

  10. Version 1.0.0

    1 download

    This model is the bilateral thigh skin rendering of a 65-year-old male with left thigh myxoid fibrosarcoma. At the time of diagnosis, the patient had metastases to his lungs. The patient therefore underwent neoadjuvant radiotherapy, surgery, and adjuvant chemotherapy and was found to have an intermediate grade lesion at the time of diagnosis. The patient is still living with the metastatic disease at 2.5 years since diagnosis. This is an STL file created from DICOM images of his CT scan which may be used for 3D printing. Myxoid fibrosarcoma (or myxoid MFH) is the most common subtype of MFH, at about 10%-20% of cases. Clinically, the tumor presents as a deep, slow-growing, painless mass. It is located more commonly in the lower extremities and retroperitoneum. Imaging on MRI demonstrates a mass with low signal intensity on T1-weighting imaging, and high signal intensity on T2-weighted imaging. On histology, a myxoid background is present with a storiform (or cartwheel) pattern seen on low-power imaging, seen in fibrosarcomas. A “myxoid background” is composed of a clear, mucoid substance. Treatment includes radiation, wide surgical resection, and chemotherapy in selected cases. However, the 5-year survival is 50%-60% depending on size, grade, depth and presence of metastasis. The term “malignant fibrous histiocytoma” was coined in the 1960s by Margaret R. Murray when histology a sarcoma demonstrated an appearance like histiocytes, with characteristics of phagocytosis and a pleomorphic pattern. With further research, this entity was identified to have a wider range of appearances with a fibrous characteristic. Today, these sarcomas are known as “pleomorphic sarcomas.” Recently, a change in the understanding of soft tissue tumors has purported that MFH is not a specific type of cancer, but a common morphologic pattern shared by unrelated tumors. One school of thought states that this morphologic pattern is shared by tumors as a common final pathway in cancer progression whereas another school of thought believes that true pleomorphic sarcomas are the result of a transformation from mesenchymal stem cells. Future research into understanding the pathway of these sarcomas and progression will help to target specific therapies and, hopefully, eventual cures. This model was created from the file STS_022.

    Free

  11. Version 1.0.0

    1 download

    This model is the left thigh muscle rendering of a 65-year-old male with left thigh myxoid fibrosarcoma. At the time of diagnosis, the patient had metastases to his lungs. The patient therefore underwent neoadjuvant radiotherapy, surgery, and adjuvant chemotherapy and was found to have an intermediate grade lesion at the time of diagnosis. The patient is still living with the metastatic disease at 2.5 years since diagnosis. This is an STL file created from DICOM images of his CT scan which may be used for 3D printing. Myxoid fibrosarcoma (or myxoid MFH) is the most common subtype of MFH, at about 10%-20% of cases. Clinically, the tumor presents as a deep, slow-growing, painless mass. It is located more commonly in the lower extremities and retroperitoneum. Imaging on MRI demonstrates a mass with low signal intensity on T1-weighting imaging, and high signal intensity on T2-weighted imaging. On histology, a myxoid background is present with a storiform (or cartwheel) pattern seen on low-power imaging, seen in fibrosarcomas. A “myxoid background” is composed of a clear, mucoid substance. Treatment includes radiation, wide surgical resection, and chemotherapy in selected cases. However, the 5-year survival is 50%-60% depending on size, grade, depth and presence of metastasis. The term “malignant fibrous histiocytoma” was coined in the 1960s by Margaret R. Murray when histology a sarcoma demonstrated an appearance like histiocytes, with characteristics of phagocytosis and a pleomorphic pattern. With further research, this entity was identified to have a wider range of appearances with a fibrous characteristic. Today, these sarcomas are known as “pleomorphic sarcomas.” Recently, a change in the understanding of soft tissue tumors has purported that MFH is not a specific type of cancer, but a common morphologic pattern shared by unrelated tumors. One school of thought states that this morphologic pattern is shared by tumors as a common final pathway in cancer progression whereas another school of thought believes that true pleomorphic sarcomas are the result of a transformation from mesenchymal stem cells. Future research into understanding the pathway of these sarcomas and progression will help to target specific therapies and, hopefully, eventual cures. This model was created from the file STS_022.

    Free

  12. Version 1.0.0

    1 download

    This model is the bilateral thigh rendering of a 49-year-old male with a right medial thigh undifferentiated pleomorphic malignant fibrous histiocytoma (MFH). The patient underwent neoadjuvant radiotherapy, surgery, and adjuvant chemotherapy treatment and was found to have a high-grade lesion at the time of diagnosis. Metastases to his lungs were also found at diagnosis. The patient is still living with the disease at 2 years since diagnosis. This is an STL file created from DICOM images of his CT scan which may be used for 3D printing. Undifferentiated pleomorphic MFH has more recently been classified as Undifferentiated Pleomorphic Sarcoma. This is the most common soft tissue sarcoma in late adulthood, commonly occurring between 55 to 80 years old and most commonly in Caucasian males. Clinically, it presents as a slow growing mass in the extremities. Biopsy of the lesion demonstrates, as its name implies, an undifferentiated and pleomorphic appearance. Pleomorphism is the pathologic description of cells and nuclei with variability in size, shape and staining, which is characteristic of a malignant neoplasm. “Undifferentiated” means that the tissue does not appear like an identifiable tissue structure. Treatment consists of wide resection and radiation. Chemotherapy is added in cases of metastasis, most commonly to the lung. Five-year survival is between 35-60% depending on grade of tumor and metastases. This model was created from the file STS_021.

    Free

  13. Version 1.0.0

    2 downloads

    This is a 3D printable STL medical file converted from a CT scan DICOM dataset of a 78-year old female that was presented by left thigh swelling( note the difference in contour between both sides), pathological examination revealed it to be malignant fibrous histiocytosis ( pleomorphic sarcoma) of high grade malignancy. The patient underwent MRI and PET scan 7 and 8 days after the pathological examination respectively. Her treatment plan was combined surgical excision and radiotherapy. 66 days later she developed regional recurrence. After 377 days of follow up, The patient was alive with disease. ( STS-020)

    Free

  14. Version 1.0.0

    1 download

    This is a 3D printable STL file converted from a CT scan DICOM dataset of a 54-year old male patient that was presented by a left thigh swelling. Histopathological examination revealed it to be extra-skeletal Ewing sarcoma of high grade of malignancy. 10 days prior to the diagnosis, the patient underwent MRI. 21 days after the diagnosis had been made the patient underwent PET scan examination as a part of his metastatic workup.His treatment plan was a combined chemotherapy/surgical resection of the tumor. 525 days later, the patient developed lung metastasis. 265 days later, the patient died.(STS-017)

    Free

  15. Version 1.0.0

    2 downloads

    This is a 3D printable medical file converted from a CT scan DICOM dataset of a 68-year old male presented by a swelling at the posterior aspect of the left pelvic region(notice the contour bulge at the posterior aspect of the left side). Histopathological examination revealed the swelling to be leiomyosarcoma of intermediate grade of malignancy. His work up included MRI and PET scan 3 and 24 days after the pathological examination respectively. His treatment plan was a combined radiotherapy/surgical resection of the tumor. 96 days later, the patient developed lung metastasis. He died after 607 days.(STS-018)

    Free

  16. Version 1.0.0

    4 downloads

    This is a 3D printable STL medical file converted from a CT scan DICOM dataset of a 78-year old female that was presented by left thigh swelling, Pathological examination revealed it to be malignant fibrous histiocytosis ( pleomorphic sarcoma) of high grade malignancy. The patient underwent MRI and PET scan 7 and 8 days after the pathological examination respectively. The patient underwent combined surgical excision/radiotherapy. 66 days later the patient developed regional recurrence. After 377 days of follow up, The patient was alive with disease. ( STS-020)

    Free

  17. Version 1.0.0

    1 download

    This is a 3D printable medical file of a CT scan DICOM dataset of a 48-year old female that was presented by right hand swelling, pathological examination revealed it to be undifferentiated malignant fibrous histiocystosis of high grade of malignancy. 28 days prior to the pathological examination, the patient underwent MRI. 30 days after the diagnosis had been made, the patient underwent PET scan. Her treatment plan was combined surgical excision/radiotherapy. after 1082 days of follow up, the patient showed no evidence of disease.(STS_019)

    Free

  18. Version 1.0.0

    1 download

    This model is the right thigh muscle rendering of a 49-year-old male with a right medial thigh undifferentiated pleomorphic malignant fibrous histiocytoma (MFH). The patient underwent neoadjuvant radiotherapy, surgery, and adjuvant chemotherapy treatment and was found to have a high-grade lesion at the time of diagnosis. Metastases to his lungs were also found at diagnosis. The patient is still living with the disease at 2 years since diagnosis. This is an STL file created from DICOM images of his CT scan which may be used for 3D printing. Undifferentiated pleomorphic MFH has more recently been classified as Undifferentiated Pleomorphic Sarcoma. This is the most common soft tissue sarcoma in late adulthood, commonly occurring between 55 to 80 years old and most commonly in Caucasian males. Clinically, it presents as a slowly growing mass in the extremities. Biopsy of the lesion demonstrates, as its name implies, an undifferentiated and pleomorphic appearance. Pleomorphism is the pathologic description of cells and nuclei with variability in size, shape, and staining, which is characteristic of a malignant neoplasm. “Undifferentiated” means that the tissue does not appear like an identifiable tissue structure. Treatment consists of wide resection and radiation. Chemotherapy is added in cases of metastasis, most commonly to the lung. Five-year survival is between 35-60% depending on the grade of tumor and metastases. This model was created from the file STS_021.

    Free

  19. Version 1.0.0

    1 download

    This model is the right thigh muscle rendering of a 49-year-old male with a right medial thigh undifferentiated pleomorphic malignant fibrous histiocytoma (MFH). The patient underwent neoadjuvant radiotherapy, surgery, and adjuvant chemotherapy treatment and was found to have a high grade lesion at the time of diagnosis. Metastases to his lungs were also found at diagnosis. The patient is still living with the disease at 2 years since diagnosis. This is an STL file created from DICOM images of his CT scan which may be used for 3D printing. Undifferentiated pleomorphic MFH has more recently been classified as Undifferentiated Pleomorphic Sarcoma. This is the most common soft tissue sarcoma in late adulthood, commonly occurring between 55 to 80 years old and most commonly in Caucasian males. Clinically, it presents as a slowly growing mass in the extremities. Biopsy of the lesion demonstrates, as its name implies, an undifferentiated and pleomorphic appearance. Pleomorphism is the pathologic description of cells and nuclei with variability in size, shape, and staining, which is characteristic of a malignant neoplasm. “Undifferentiated” means that the tissue does not appear like an identifiable tissue structure. Treatment consists of wide resection and radiation. Chemotherapy is added in cases of metastasis, most commonly to the lung. Five-year survival is between 35-60% depending on the grade of tumor and metastases. This model was created from the file STS_021.

    Free

  20. Version 1.0.0

    3 downloads

    This is a case of left thigh posterior mass in a 75-year old female patient. Pathological examination of the specimen revealed spindle shaped cells suggestive of liposarcoma with intermediate grade of malignancy. MRI was done for this patient 33 days before taking the biopsy, and a week after confirming the diagnosis a PET scan was done as a part of the metastatic workup. After performing surgical resection of the tumor followed by radiotherapy, the patient showed no evidence of recurrence for 760 days of follow up. This is a 3D printable medical STL file converted from the real CT scan DICOM dataset of this patient(STS-016).

    Free

  21. Version 1.0.0

    4 downloads

    This is a 3D-printable medical file extracted from the DICOM dataset of a 34-year old female with right thigh swelling. Histo-pathological examination revealed it to be a synovial sarcoma of intermediate grade. 13 days prior to the definitive diagnosis, MRI was done for this patient. 23 days later PET scan was also done as a part of her metastatic workup. After treating the patient with radiotherapy and surgical resection, The patient showed no evidence of disease after nearly 2 years of follow up. (STS-015)

    Free

  22. Version 1.0.0

    1 download

    This model is the bilateral thigh muscle rendering of a 56 year old male with a pleomorphic leiomyosarcoma of the anterior compartment of the right thigh. The patient underwent neoadjuvant radiotherapy, surgery, and adjuvant chemotherapy treatment and was found to have an intermediate grade lesion at the time of diagnosis. However, the tumor metastasized to his lungs, and the patient died 2.5 years after diagnosis. This is an STL file created from DICOM images of his CT scan which may be used for 3D printing. Leiomyosarcomas are aggressive soft tissue malignancies that are thought to arise from the smooth muscle cells lining small blood vessels. Pleomorphism is the pathologic description of cells and nuclei with variability in size, shape and staining, which is characteristic of a malignant neoplasm. Pleomorphic leiomyosarcoma is an aggressive form of leiomyosarcoma, accounting for approximately 10% of these tumors. The mean age of occurrence is 58 years old, with a range from 31-89 years. These usually occur in the extremities, but may also present in the retroperitoneum/abdominal cavity, chest/abdominal wall, and, occasionally, the scalp. On biopsy, the definition of pleomorphic leiomyosarcoma is the presence of pleomorphic cells in at last two-thirds of the cut section and at least one section of positive staining for smooth muscle. Treatment is early wide resection of the primary lesion and neo-adjuvant or adjuvant chemotherapy and radiation. Tumors may metastasize to the lung. A large primary tumor and presence in the retroperitoneal cavity are poor predictive factors, and about 65% of patients succumb to the disease. This model was created from the file STS_014.

    Free

  23. Version 1.0.0

    5 downloads

    This model is the right thigh muscle rendering of a 56 year old male with a pleomorphic leiomyosarcoma of the anterior compartment of the right thigh. The patient underwent neoadjuvant radiotherapy, surgery, and adjuvant chemotherapy treatment and was found to have an intermediate grade lesion at the time of diagnosis. However, the tumor metastasized to his lungs, and the patient died 2.5 years after diagnosis. This is an STL file created from DICOM images of his CT scan which may be used for 3D printing. Leiomyosarcomas are aggressive soft tissue malignancies that are thought to arise from the smooth muscle cells lining small blood vessels. Pleomorphism is the pathologic description of cells and nuclei with variability in size, shape and staining, which is characteristic of a malignant neoplasm. Pleomorphic leiomyosarcoma is an aggressive form of leiomyosarcoma, accounting for approximately 10% of these tumors. The mean age of occurrence is 58 years old, with a range from 31-89 years. These usually occur in the extremities, but may also present in the retroperitoneum/abdominal cavity, chest/abdominal wall, and, occasionally, the scalp. On biopsy, the definition of pleomorphic leiomyosarcoma is the presence of pleomorphic cells in at last two-thirds of the cut section and at least one section of positive staining for smooth muscle. Treatment is early wide resection of the primary lesion and neo-adjuvant or adjuvant chemotherapy and radiation. Tumors may metastasize to the lung. A large primary tumor and presence in the retroperitoneal cavity are poor predictive factors, and about 65% of patients succumb to the disease. This model was created from the file STS_014.

    Free

  24. Version 1.0.0

    0 downloads

    This is a 3D model of a right thigh soft tissue mass extracted from the ct scan DICOM dataset of a 62-year old female. Histopathological examination revealed the mass to be sclerosing epithelioid fibrosarcoma of intermediate grade. 14 days prior to the pathological examination, MRI was done for this patient and 40 days after the diagnosis a PET scan was done.Her treatment plan was a combination of surgical resection of the mass and radiotherapy. Bone metastasis was confirmed 235 days after the initial diagnosis.The patient died 428 days after the diagnosis of the bone metastasis. (STS-012)

    Free

  25. Version 1.0.0

    3 downloads

    This is a case of 56-year old female patient with right thigh swelling, histo-pathology revealed it to be solitary fibrous tumor of the right thigh with intermediate grade of malignancy. MRI and PET scan were done for this patient after the initial diagnosis by 3 and 36 days respectively. Her treatment plan included radiotherapy and surgical resection of the tumor combined. upon 637 days of follow up , the patient showed no evidence of disease (NED). This STL file had been created from a CT scan DICOM dataset and is availabe for medical 3D printing .

    Free

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