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1.
Am Surg ; 69(9): 779-83, 2003 Sep.
Article in English | MEDLINE | ID: mdl-14509326

ABSTRACT

The management of metastasis from parathyroid carcinoma (PC) is an unusual challenge. Systemic therapy has minimal effect on the course of the disease and its associated hypercalcemia. Resection of isolated pulmonary metastases is an attractive option in the setting of recurrent hypercalcemia. We report a case of a patient who underwent resection of multiple functional PC pulmonary metastases almost 20 years after the original neck resection. The patient originally presented in 1982 with what was thought to be hyperparathyroidism secondary to a parathyroid adenoma. Surgical exploration revealed the presence of a well differentiated PC. The patient was transiently normocalcemic, but underwent surgical exploration in 1993 and 1996 for recurrent PC in the neck. The patient again improved, but presented in 2001 with diffuse arthralgia, fatigue, malaise, weight loss, and decreased appetite. She was found to have a serum calcium of 12.7 mg/dL and an intact parathyroid hormone of 1542 pmol/L. Computed tomography identified the presence of two right-sided and two left-sided pulmonary masses. Sternotomy with bilateral pulmonary metastectomy was performed. Functional PC metastasis was confirmed on pathological examination. One year following metastectomy the patient is hypocalcemic, requiring oral calcium and vitamin D supplementation. Functional pulmonary metastasis from PC is a rare cause of hypercalcemia. Complete resection of isolated pulmonary metastases can provide effective palliation with long-term survival.


Subject(s)
Lung Neoplasms/secondary , Lung Neoplasms/surgery , Neoplasm Recurrence, Local/surgery , Parathyroid Neoplasms/pathology , Adult , Diagnosis, Differential , Female , Humans , Hypercalcemia/etiology , Lung Neoplasms/diagnostic imaging , Neoplasm Recurrence, Local/complications , Parathyroid Neoplasms/complications , Parathyroid Neoplasms/surgery , Tomography, X-Ray Computed , Treatment Outcome
2.
Leuk Lymphoma ; 44(8): 1413-6, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12952237

ABSTRACT

Helicobacter pylori have been causally linked to primary gastric B-cell lymphoma of the mucosa-associated lymphoid tissue (MALT) type. Antibiotic therapy to eradicate H. pylori has been shown to induce remission of such lymphoma. We report a case of primary B-cell MALT lymphoma of the jejunum associated with H. pylori. The literature of intestinal MALT lymphoma is reviewed.


Subject(s)
Helicobacter Infections/complications , Jejunal Neoplasms/virology , Lymphoma, B-Cell, Marginal Zone/virology , Combined Modality Therapy , Disease-Free Survival , Female , Helicobacter Infections/diagnosis , Helicobacter pylori , Humans , Jejunal Neoplasms/diagnosis , Jejunal Neoplasms/therapy , Lymphoma, B-Cell, Marginal Zone/diagnosis , Lymphoma, B-Cell, Marginal Zone/therapy , Middle Aged , Remission Induction/methods
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