Hypercalcemia Associated with Extramammary Paget’s Disease
Hypercalcemia of malignancy occurs in up to one third of patients at some point during the course of their advanced stage. The majority of them is caused by humoral hypercalcemia of malignancy due to systemic secretion of parathyroid hormone–related protein (PTHrP) by tumor cells. Extramammary Paget...
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Published in | Case reports in oncology Vol. 13; no. 3; pp. 1209 - 1214 |
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Main Authors | , , , , , , |
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Language | English |
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S. Karger AG
01.09.2020
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Abstract | Hypercalcemia of malignancy occurs in up to one third of patients at some point during the course of their advanced stage. The majority of them is caused by humoral hypercalcemia of malignancy due to systemic secretion of parathyroid hormone–related protein (PTHrP) by tumor cells. Extramammary Paget’s disease is a slow-growing cutaneous malignancy commonly limited to the epidermis of the anogenital region, but rarely becomes invasive and metastatic to distant sites. Herein, we report a 70-year-old male patient with metastatic extramammary Paget’s disease. He consulted our hospital with altered consciousness and tumor in his genital area. Physical examination revealed erythematous plaque with a tumor on the scrotum and perineum. It was diagnosed as extramammary Paget’s disease (multiple liver metastases and multiple lymph node metastases by skin biopsy and image examination). Increases in serum-corrected calcium and PTHrP-intact levels (15.3 mg/dL and 66.1 pg/L, respectively) were confirmed. PTHrP immunohistochemistry showed positive staining in the tumor cells. We diagnosed humoral hypercalcemia of malignancy. We treated hypercalcemia with saline, furosemide, zoledronic acid, and elcatonin. Regarding the local control of the tumor, 30 Gy/10 Fr electron beam therapy was performed. However, treatment with zoledronic acid was only temporally effective to correct hypercalcemia, and an increased serum calcium level developed again. Concurrently, the liver metastases were rapidly enlarged, and his general condition gradually deteriorated. The patient died on day 55. When patients with extramammary Paget’s disease show unconsciousness, serum calcium level should be measured and PTHrP-producing tumor distinguished. |
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AbstractList | Hypercalcemia of malignancy occurs in up to one third of patients at some point during the course of their advanced stage. The majority of them is caused by humoral hypercalcemia of malignancy due to systemic secretion of parathyroid hormone–related protein (PTHrP) by tumor cells. Extramammary Paget’s disease is a slow-growing cutaneous malignancy commonly limited to the epidermis of the anogenital region, but rarely becomes invasive and metastatic to distant sites. Herein, we report a 70-year-old male patient with metastatic extramammary Paget’s disease. He consulted our hospital with altered consciousness and tumor in his genital area. Physical examination revealed erythematous plaque with a tumor on the scrotum and perineum. It was diagnosed as extramammary Paget’s disease (multiple liver metastases and multiple lymph node metastases by skin biopsy and image examination). Increases in serum-corrected calcium and PTHrP-intact levels (15.3 mg/dL and 66.1 pg/L, respectively) were confirmed. PTHrP immunohistochemistry showed positive staining in the tumor cells. We diagnosed humoral hypercalcemia of malignancy. We treated hypercalcemia with saline, furosemide, zoledronic acid, and elcatonin. Regarding the local control of the tumor, 30 Gy/10 Fr electron beam therapy was performed. However, treatment with zoledronic acid was only temporally effective to correct hypercalcemia, and an increased serum calcium level developed again. Concurrently, the liver metastases were rapidly enlarged, and his general condition gradually deteriorated. The patient died on day 55. When patients with extramammary Paget’s disease show unconsciousness, serum calcium level should be measured and PTHrP-producing tumor distinguished. Hypercalcemia of malignancy occurs in up to one third of patients at some point during the course of their advanced stage. The majority of them is caused by humoral hypercalcemia of malignancy due to systemic secretion of parathyroid hormone-related protein (PTHrP) by tumor cells. Extramammary Paget's disease is a slow-growing cutaneous malignancy commonly limited to the epidermis of the anogenital region, but rarely becomes invasive and metastatic to distant sites. Herein, we report a 70-year-old male patient with metastatic extramammary Paget's disease. He consulted our hospital with altered consciousness and tumor in his genital area. Physical examination revealed erythematous plaque with a tumor on the scrotum and perineum. It was diagnosed as extramammary Paget's disease (multiple liver metastases and multiple lymph node metastases by skin biopsy and image examination). Increases in serum-corrected calcium and PTHrP-intact levels (15.3 mg/dL and 66.1 pg/L, respectively) were confirmed. PTHrP immunohistochemistry showed positive staining in the tumor cells. We diagnosed humoral hypercalcemia of malignancy. We treated hypercalcemia with saline, furosemide, zoledronic acid, and elcatonin. Regarding the local control of the tumor, 30 Gy/10 Fr electron beam therapy was performed. However, treatment with zoledronic acid was only temporally effective to correct hypercalcemia, and an increased serum calcium level developed again. Concurrently, the liver metastases were rapidly enlarged, and his general condition gradually deteriorated. The patient died on day 55. When patients with extramammary Paget's disease show unconsciousness, serum calcium level should be measured and PTHrP-producing tumor distinguished.Hypercalcemia of malignancy occurs in up to one third of patients at some point during the course of their advanced stage. The majority of them is caused by humoral hypercalcemia of malignancy due to systemic secretion of parathyroid hormone-related protein (PTHrP) by tumor cells. Extramammary Paget's disease is a slow-growing cutaneous malignancy commonly limited to the epidermis of the anogenital region, but rarely becomes invasive and metastatic to distant sites. Herein, we report a 70-year-old male patient with metastatic extramammary Paget's disease. He consulted our hospital with altered consciousness and tumor in his genital area. Physical examination revealed erythematous plaque with a tumor on the scrotum and perineum. It was diagnosed as extramammary Paget's disease (multiple liver metastases and multiple lymph node metastases by skin biopsy and image examination). Increases in serum-corrected calcium and PTHrP-intact levels (15.3 mg/dL and 66.1 pg/L, respectively) were confirmed. PTHrP immunohistochemistry showed positive staining in the tumor cells. We diagnosed humoral hypercalcemia of malignancy. We treated hypercalcemia with saline, furosemide, zoledronic acid, and elcatonin. Regarding the local control of the tumor, 30 Gy/10 Fr electron beam therapy was performed. However, treatment with zoledronic acid was only temporally effective to correct hypercalcemia, and an increased serum calcium level developed again. Concurrently, the liver metastases were rapidly enlarged, and his general condition gradually deteriorated. The patient died on day 55. When patients with extramammary Paget's disease show unconsciousness, serum calcium level should be measured and PTHrP-producing tumor distinguished. |
Author | Aoyama, Yumi Fujimoto, Wataru Kamitani, Nobuhiko Sato, Tetsuko Yamamoto, Takenobu Tanaka, Ryo Wada, Yoshihisa |
AuthorAffiliation | a Department of Dermatology, Kawasaki Medical School, Kurashiki, Japan c Department of Radiation Oncology, Kawasaki Medical School, Kurashiki, Japan b Department of Nephrology/Hypertension, Kawasaki Medical School, Kurashiki, Japan |
AuthorAffiliation_xml | – name: a Department of Dermatology, Kawasaki Medical School, Kurashiki, Japan – name: c Department of Radiation Oncology, Kawasaki Medical School, Kurashiki, Japan – name: b Department of Nephrology/Hypertension, Kawasaki Medical School, Kurashiki, Japan |
Author_xml | – sequence: 1 givenname: Tetsuko surname: Sato fullname: Sato, Tetsuko – sequence: 2 givenname: Yoshihisa surname: Wada fullname: Wada, Yoshihisa – sequence: 3 givenname: Nobuhiko surname: Kamitani fullname: Kamitani, Nobuhiko – sequence: 4 givenname: Takenobu surname: Yamamoto fullname: Yamamoto, Takenobu – sequence: 5 givenname: Yumi orcidid: 0000-0003-3701-5575 surname: Aoyama fullname: Aoyama, Yumi – sequence: 6 givenname: Wataru surname: Fujimoto fullname: Fujimoto, Wataru – sequence: 7 givenname: Ryo surname: Tanaka fullname: Tanaka, Ryo email: *Ryo Tanaka, Kawasaki Medical School Department of Dermatology, 577 Matsushima, Kurashiki, Okayama 701-0192 (Japan), ryot@med.kawasaki-m.ac.jp |
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Cites_doi | 10.2169/internalmedicine.55.7134 10.1200/jop.2016.011155 10.4103/1947-2714.170600 10.1016/j.canep.2015.10.012 10.3389/fonc.2018.00047 10.11005/jbm.2017.24.4.249 10.1056/nejmcp042806 10.1177/1078155213518361 |
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Keywords | Hypercalcemia Extramammary Paget’s disease Behavioral disturbance Parathyroid hormone-related protein |
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References | Sakamoto M, Koh S, Tatsuoka Y, Katsuyama E, Katakami H. A case of PTHrP producing extramammary Paget’s disease. Horm Rinsho. 1997 Nov;45(11 Suppl l):131–3. (in Japanese) Ashihara N, Nakajima K, Nakamura Y, Kobayashi M, Shirahata K, Maeda C, . Denosumab is effective for controlling serum calcium levels in patients with humoral hypercalcemia of malignancy syndrome: a case report on parathyroid hormone-related protein-producing cholangiocarcinoma. Intern Med, 2016 Dec;55(23):3453–7. Mirrakhimov AE. Hypercalcemia of malignancy: An update on pathogenesis and management. N Am J Med Sci. 2015 Nov;7(11):483–93. Fukuda K, Funakoshi T. Metastatic extramammary Paget's disease: pathogenesis and novel therapeutic approach. Front Oncol. 2018 Feb;8:38. Goldner W, More S. Treating cancer-related hypercalcemia with gallium nitrate. J Support Oncol. 2016 May;2(6):509–16. Jick S, Li L, Gastanaga VM, Liede A. Prevalence of hypercalcemia of malignancy among cancer patients in the UK: Analysis of the Clinical Practice Research Datalink database. Cancer Epidemiol. 2015 Dec; 39(6):901–7. Dietzek A, Connelly K, Cotugno M, Bartel S, McDonnell AM. Denosumab in hypercalcemia of malignancy: a case series. J Oncol Pharm Pract. 2015 Apr;21(2):143–7. Jin J, Chung JO, Chung MY, Cho DH, Chung DJ. Clinical characteristics, causes and survival in 115 cancer patients with parathyroid hormone related protein-mediated hypercalcemia. J Bone Metab. 2017 Nov; 24(4):249–55. Hirano K, Uchiyama T, Yamaguchi Y, Okonogi H, Ikeda M, Yokoyama K, . A case of PTHrP producing extramammary Paget’s disease. J Jpn Soc Dial Ther. 2008 May;41(Suppl 1):780. (in Japanese) Stewart AF. Clinical practice. Hypercalcemia associated with cancer. N Engl J Med. 2005 Jan;352(4):373–9. ref8 ref7 ref4 ref3 ref6 ref5 ref2 ref1 |
References_xml | – reference: Ashihara N, Nakajima K, Nakamura Y, Kobayashi M, Shirahata K, Maeda C, . Denosumab is effective for controlling serum calcium levels in patients with humoral hypercalcemia of malignancy syndrome: a case report on parathyroid hormone-related protein-producing cholangiocarcinoma. Intern Med, 2016 Dec;55(23):3453–7. – reference: Sakamoto M, Koh S, Tatsuoka Y, Katsuyama E, Katakami H. A case of PTHrP producing extramammary Paget’s disease. Horm Rinsho. 1997 Nov;45(11 Suppl l):131–3. (in Japanese) – reference: Goldner W, More S. Treating cancer-related hypercalcemia with gallium nitrate. J Support Oncol. 2016 May;2(6):509–16. – reference: Mirrakhimov AE. Hypercalcemia of malignancy: An update on pathogenesis and management. N Am J Med Sci. 2015 Nov;7(11):483–93. – reference: Hirano K, Uchiyama T, Yamaguchi Y, Okonogi H, Ikeda M, Yokoyama K, . A case of PTHrP producing extramammary Paget’s disease. J Jpn Soc Dial Ther. 2008 May;41(Suppl 1):780. (in Japanese) – reference: Stewart AF. Clinical practice. Hypercalcemia associated with cancer. N Engl J Med. 2005 Jan;352(4):373–9. – reference: Fukuda K, Funakoshi T. Metastatic extramammary Paget's disease: pathogenesis and novel therapeutic approach. Front Oncol. 2018 Feb;8:38. – reference: Jin J, Chung JO, Chung MY, Cho DH, Chung DJ. Clinical characteristics, causes and survival in 115 cancer patients with parathyroid hormone related protein-mediated hypercalcemia. J Bone Metab. 2017 Nov; 24(4):249–55. – reference: Dietzek A, Connelly K, Cotugno M, Bartel S, McDonnell AM. Denosumab in hypercalcemia of malignancy: a case series. J Oncol Pharm Pract. 2015 Apr;21(2):143–7. – reference: Jick S, Li L, Gastanaga VM, Liede A. Prevalence of hypercalcemia of malignancy among cancer patients in the UK: Analysis of the Clinical Practice Research Datalink database. Cancer Epidemiol. 2015 Dec; 39(6):901–7. – ident: ref7 doi: 10.2169/internalmedicine.55.7134 – ident: ref3 doi: 10.1200/jop.2016.011155 – ident: ref2 doi: 10.4103/1947-2714.170600 – ident: ref5 doi: 10.1016/j.canep.2015.10.012 – ident: ref4 doi: 10.3389/fonc.2018.00047 – ident: ref6 doi: 10.11005/jbm.2017.24.4.249 – ident: ref1 doi: 10.1056/nejmcp042806 – ident: ref8 doi: 10.1177/1078155213518361 |
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SubjectTerms | Antigens behavioral disturbance Cancer therapies Case Report Case reports Chemotherapy extramammary paget’s disease Fractures Hypercalcemia Kidney cancer Ligands Liver Lymphatic system Medical prognosis Metastasis parathyroid hormone-related protein Pathogenesis Patients |
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Title | Hypercalcemia Associated with Extramammary Paget’s Disease |
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