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weight loss/sarkoma
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Effectiveness of nitrogen mustards in retarding the growth of sarcoma 180 with reference to route of administration, age of tumors, food intake, and weight loss of the mice.
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[70-year-old kidney transplant patient with anorexia and weight loss. Kaposi sarcoma].
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F-18 FDG PET/CT in pulmonary artery sarcoma: clinical vignette.
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Pulmonary artery sarcomas (PAS's) are extremely rare malignant tumors that arise from the endothelial lining of the pulmonary arteries. On CT scans PAS's appear as intraluminal filling defects in the pulmonary arteries, mimicking pulmonary embolism (PE). Due to the similarities in radiographic
Clinical and radiological features of pulmonary artery sarcoma: A report of nine cases.
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OBJECTIVE
To improve our understanding and facilitate early diagnosis of pulmonary artery sarcoma (PAS).
METHODS
The clinical and radiological features of 9 histopathologically confirmed patients with PAS were retrospectively analyzed.
RESULTS
Our PAS cohort consisted of 5 males and 4 females, with
Undifferentiated (embryonal) sarcoma of the liver (USL): MRI findings including dynamic gadolinium enhancement.
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We report the MR appearance of undifferentiated (embryonal) sarcoma of the liver (USL) in a 13-year-old female who presented with a 1-year history of intermittent abdominal pain, weight loss, and fatigue. The tumor was a large, solitary, well-defined focal mass lesion with multiple cystic spaces,
Small-bowel myeloid sarcoma: Report of a case with atypical presentation.
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BACKGROUND
Small-bowel myeloid sarcoma is rare. Acute bowel obstruction is its usual clinical presentation.
METHODS
We report a case of small-bowel myeloid sarcoma that occurred in a 64-year-old woman who presented chronic secretory diarrhoea, hypokalaemia, and weight loss. Immature white blood
Clear cell sarcoma of the stomach.
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Clear cell sarcoma (CCS) is a high grade soft tissue sarcoma with a distinct molecular profile. Gastrointestinal CCS is very rare and most reported cases are in adults. We describe a 10-year-old female with a 4-month history of anemia who later developed fever, weight loss and abdominal pain. She
A Rare Case of Retroperitoneal Follicular Dendritic Cell Sarcoma Identified by 99mTc-HYNIC-TOC SPECT/CT.
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Follicular dendritic cell sarcoma is a very rare neoplasm, which is not lymphoma, but originates from a type of immune cells called follicular dendritic cells. We presented a 37-year-old woman who has suffered from obstructive jaundice, weight loss and right upper abdominal pain for 2 months. The
Sarcoma of the gastrointestinal tract: a review of 40 cases.
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In a ten-year update of the Vanderbilt University Medical Center experience, cases of malignant lymphomas (20) and soft tissue sarcomas (20) of the gastrointestinal tract were reviewed. The stomach was the most common site (63%). The three most common presenting symptoms were abdominal pain, weight
Intimal pulmonary artery sarcoma presenting as severe dyspnea and right heart insufficiency.
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BACKGROUND
Pulmonary artery sarcoma is a rare tumor with a poor prognosis.
METHODS
We report the case of a 64-year-old man with an intimal pulmonary artery sarcoma presenting with severe high oxygen flow-demanding dyspnea and weight loss of 12 kg in the last 6 months. On echocardiography, right
Langerhans cell sarcoma: an unusual microscopic presentation.
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A 70-year-old Caucasian male presented to our clinic for a pruritic eruption progressing over several months. He complained of fatigue with a 20-pound weight loss over the past year. On presentation, the patient had browny-yellow to violaceous, purpuric, macular and papular lesions on the legs,
Aggressive classical Kaposi's sarcoma mimicking malignant lymphoma.
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Classical Kaposi's sarcoma is an unusual multifocal neoplasm of vascular endothelial cell origin, and considered a less malignant, slowly-progressing tumor. Although visceral involvement is occasionally seen in HIV/AIDS patients with KS, tumor dissemination to visceral lymph nodes in classical KS is
Primary lymphomas and sarcomas of the stomach.
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The records of patients with primary gastric lymphoma and sarcoma treated at M. D. Anderson Hospital and Tumor Institute between 1945 and 1975 were reviewed. Weight loss, abdominal pain, nausea, and vomiting were the most common presenting symptoms, while palpable abdominal mass was the most common
Pulmonary manifestation of a Langerhans cell sarcoma: case report and review of the literature.
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In the following, we describe the very rare case of Langerhans cell sarcoma (LCS) in the lung. Throughout the medical literature, only a few cases have been published, and, to the best of our knowledge, this is the first case to be reported in Germany. The patient was an 81-year-old man who showed
Treatment of atypical leishmaniasis with interferon gamma resulting in progression of Kaposi's sarcoma in an AIDS patient.
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Visceral leishmaniasis (kala-azar) affecting HIV-infected patient is being reported in increasing frequency. A 40-year-old German bisexual patient with full-blown AIDS is described who presented with Kaposi's sarcoma, epigastric pain, diarrhea, and weight loss but without fever. Leishmania
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