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Humoral Hypercalcemia in Uterine Cancers: A Case Report and Literature Review

Patient: Female, 53 Final Diagnosis: Endometrial stromal sarcoma Symptoms: Abdominal distension Medication: — Clinical Procedure: — Specialty: Oncology OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Paraneoplastic hypercalcemia is a well-described complication associated with a var...

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Autores principales: Nehru, Vijeyaluxmy Motilal, Garcia, Gwenalyn, Ding, Juan, Kong, Fanyi, Dai, Qun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234677/
https://www.ncbi.nlm.nih.gov/pubmed/28057913
http://dx.doi.org/10.12659/AJCR.900088
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author Nehru, Vijeyaluxmy Motilal
Garcia, Gwenalyn
Ding, Juan
Kong, Fanyi
Dai, Qun
author_facet Nehru, Vijeyaluxmy Motilal
Garcia, Gwenalyn
Ding, Juan
Kong, Fanyi
Dai, Qun
author_sort Nehru, Vijeyaluxmy Motilal
collection PubMed
description Patient: Female, 53 Final Diagnosis: Endometrial stromal sarcoma Symptoms: Abdominal distension Medication: — Clinical Procedure: — Specialty: Oncology OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Paraneoplastic hypercalcemia is a well-described complication associated with a variety of malignancies. However, its incidence in gynecological malignancies is low. CASE REPORT: A 53-year-old woman presented with progressive abdominal distention and irregular vaginal bleeding of several weeks’ duration. A contrast CT abdomen and pelvis was significant for a mass in the lower uterine/cervical region, multiple peritoneal and omental masses, enlarged pelvic and paraaortic lymph nodes, and large-volume ascites. A pelvic exam revealed a fungating vaginal mass, with biopsy showing a high-grade tumor with immunohistochemical staining positive for vimentin, CD10, and cyclin D1, consistent with endometrial stromal sarcoma. During her hospitalization, the patient became increasingly lethargic. Workup showed severe hypercalcemia and evidence of acute kidney injury. The patient did not have evidence of bony metastatic disease on imaging studies. Further laboratory evaluation revealed an elevated PTHrP of 301 pg/mL (nl 14–27), a depressed PTH level of 3 pg/mL (nl 15–65), and a depressed 25-OH vitamin D level of 16 ng/mL (nl 30–100), consistent with humoral hypercalcemia of malignancy. The patient was treated with pamidronate, calcitonin, and intravenous fluids. She eventually required temporary hemodialysis and denosumab for refractory hypercalcemia, which improved her electrolyte abnormalities and clinical status. CONCLUSIONS: Uterine malignancies of various histologies are increasingly recognized as a cause of humoral hypercalcemia. They are an important differential diagnosis in a woman with hypercalcemia and abnormal vaginal bleeding or abdominal symptoms.
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spelling pubmed-52346772017-01-18 Humoral Hypercalcemia in Uterine Cancers: A Case Report and Literature Review Nehru, Vijeyaluxmy Motilal Garcia, Gwenalyn Ding, Juan Kong, Fanyi Dai, Qun Am J Case Rep Articles Patient: Female, 53 Final Diagnosis: Endometrial stromal sarcoma Symptoms: Abdominal distension Medication: — Clinical Procedure: — Specialty: Oncology OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Paraneoplastic hypercalcemia is a well-described complication associated with a variety of malignancies. However, its incidence in gynecological malignancies is low. CASE REPORT: A 53-year-old woman presented with progressive abdominal distention and irregular vaginal bleeding of several weeks’ duration. A contrast CT abdomen and pelvis was significant for a mass in the lower uterine/cervical region, multiple peritoneal and omental masses, enlarged pelvic and paraaortic lymph nodes, and large-volume ascites. A pelvic exam revealed a fungating vaginal mass, with biopsy showing a high-grade tumor with immunohistochemical staining positive for vimentin, CD10, and cyclin D1, consistent with endometrial stromal sarcoma. During her hospitalization, the patient became increasingly lethargic. Workup showed severe hypercalcemia and evidence of acute kidney injury. The patient did not have evidence of bony metastatic disease on imaging studies. Further laboratory evaluation revealed an elevated PTHrP of 301 pg/mL (nl 14–27), a depressed PTH level of 3 pg/mL (nl 15–65), and a depressed 25-OH vitamin D level of 16 ng/mL (nl 30–100), consistent with humoral hypercalcemia of malignancy. The patient was treated with pamidronate, calcitonin, and intravenous fluids. She eventually required temporary hemodialysis and denosumab for refractory hypercalcemia, which improved her electrolyte abnormalities and clinical status. CONCLUSIONS: Uterine malignancies of various histologies are increasingly recognized as a cause of humoral hypercalcemia. They are an important differential diagnosis in a woman with hypercalcemia and abnormal vaginal bleeding or abdominal symptoms. International Scientific Literature, Inc. 2017-01-06 /pmc/articles/PMC5234677/ /pubmed/28057913 http://dx.doi.org/10.12659/AJCR.900088 Text en © Am J Case Rep, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
spellingShingle Articles
Nehru, Vijeyaluxmy Motilal
Garcia, Gwenalyn
Ding, Juan
Kong, Fanyi
Dai, Qun
Humoral Hypercalcemia in Uterine Cancers: A Case Report and Literature Review
title Humoral Hypercalcemia in Uterine Cancers: A Case Report and Literature Review
title_full Humoral Hypercalcemia in Uterine Cancers: A Case Report and Literature Review
title_fullStr Humoral Hypercalcemia in Uterine Cancers: A Case Report and Literature Review
title_full_unstemmed Humoral Hypercalcemia in Uterine Cancers: A Case Report and Literature Review
title_short Humoral Hypercalcemia in Uterine Cancers: A Case Report and Literature Review
title_sort humoral hypercalcemia in uterine cancers: a case report and literature review
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234677/
https://www.ncbi.nlm.nih.gov/pubmed/28057913
http://dx.doi.org/10.12659/AJCR.900088
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