Acromegaly and a Giant Retroperitoneal Liposarcoma Producing IGF-1
ABSTRACT: Objective: Liposarcoma is the most common histotype of retroperitoneal sarcomas, representing up to 45% of all cases. We report a rare combination of acromegaly and liposarcoma in the same individual. Methods: Laboratory and imaging studies including an oral glucose tolerance test, measur...
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doaj-af5725f8afcb4610b14b12396062a8c02021-04-30T07:23:11ZengElsevierAACE Clinical Case Reports2376-06052020-07-0164e165e169Acromegaly and a Giant Retroperitoneal Liposarcoma Producing IGF-1César Ernesto Lam-Chung, MD0Diana Lizbeth Rodríguez-Orihuela, MD1Rebeca Arízaga-Ramírez, MD2Paloma Almeda-Valdés, MD, PhD3Ana Karen Castillo-Valdez, HT4Kassandra Magaña-Pérez, MD5José Luis Ventura-Gallegos, MS6Armando Gamboa-Domínguez, MD7Jazmín De Anda González, MD8Franciscoc J. Gómez-Pérez, MD9Daniel Cuevas-Ramos, MD10From the Neuroendocrinology Clinic, Department of Endocrinology and MetabolismDepartment of PathologyDepartment of Radiology, Salvador Zubirán National Institute of Health Sciences and Nutrition, Mexico City, Mexico.From the Neuroendocrinology Clinic, Department of Endocrinology and MetabolismDepartment of PathologyFrom the Neuroendocrinology Clinic, Department of Endocrinology and MetabolismFrom the Neuroendocrinology Clinic, Department of Endocrinology and MetabolismDepartment of PathologyDepartment of PathologyFrom the Neuroendocrinology Clinic, Department of Endocrinology and MetabolismFrom the Neuroendocrinology Clinic, Department of Endocrinology and Metabolism; Address correspondence to Dr. Daniel Cuevas-Ramos, Neuroendocrinology Clinic. Department of Endocrinology and Metabolism. Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán. Vasco de Quiroga 15, Belisario Domínguez Sección XVI, Tlalpan 14080. Mexico City, Mexico.ABSTRACT: Objective: Liposarcoma is the most common histotype of retroperitoneal sarcomas, representing up to 45% of all cases. We report a rare combination of acromegaly and liposarcoma in the same individual. Methods: Laboratory and imaging studies including an oral glucose tolerance test, measurements of growth hormone (GH) and insulin-like growth factor-1 (IGF-1), and a computed tomography scan were performed. Results: The patient was a 60-year-old male with a history of acromegaly diagnosed on the basis of elevated IGF-1 at 1,373 ng/mL (age-appropriate reference range is 87 to 225 ng/mL) and macroadenoma treated with transsphenoidal surgery. He presented 8 years later with a history of abdominal distension and weight loss. Physical examination was notable for a right-sided abdominal mass that was tense and non-fluctuant. Two years earlier, he had a post oral glucose tolerance test GH level <0.25 ng/mL and IGF-1 level of 256 ng/mL (age-appropriate reference range is 55 to 206 ng/mL). Pituitary magnetic resonance imaging reported a 3.7 × 2.0-mm left-sided parasagittal lesion. Computed tomography scan showed a 25.0 × 22.0 × 32.3-cm heterogeneous giant mass in the right abdomen corresponding to a liposarcoma causing displacement of kidney, liver, and bowel loops. The patient was treated with a complete en bloc resection of the liposarcoma with the right kidney (45 × 33 × 17 cm) and tumor (9,400 g). Immunohistochemical examination revealed positive IGF-1 and GH staining. The patient suffered postoperative gastrointestinal bleeding that resulted in hemorrhagic shock and died on the 29th postoperative day after a cardiorespiratory arrest. Conclusion: Acromegalic patients are at increased risk of developing various types of neoplasms. This is the first documented coexistence of liposarcoma and history of acromegaly.http://www.sciencedirect.com/science/article/pii/S2376060520300092 |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
César Ernesto Lam-Chung, MD Diana Lizbeth Rodríguez-Orihuela, MD Rebeca Arízaga-Ramírez, MD Paloma Almeda-Valdés, MD, PhD Ana Karen Castillo-Valdez, HT Kassandra Magaña-Pérez, MD José Luis Ventura-Gallegos, MS Armando Gamboa-Domínguez, MD Jazmín De Anda González, MD Franciscoc J. Gómez-Pérez, MD Daniel Cuevas-Ramos, MD |
spellingShingle |
César Ernesto Lam-Chung, MD Diana Lizbeth Rodríguez-Orihuela, MD Rebeca Arízaga-Ramírez, MD Paloma Almeda-Valdés, MD, PhD Ana Karen Castillo-Valdez, HT Kassandra Magaña-Pérez, MD José Luis Ventura-Gallegos, MS Armando Gamboa-Domínguez, MD Jazmín De Anda González, MD Franciscoc J. Gómez-Pérez, MD Daniel Cuevas-Ramos, MD Acromegaly and a Giant Retroperitoneal Liposarcoma Producing IGF-1 AACE Clinical Case Reports |
author_facet |
César Ernesto Lam-Chung, MD Diana Lizbeth Rodríguez-Orihuela, MD Rebeca Arízaga-Ramírez, MD Paloma Almeda-Valdés, MD, PhD Ana Karen Castillo-Valdez, HT Kassandra Magaña-Pérez, MD José Luis Ventura-Gallegos, MS Armando Gamboa-Domínguez, MD Jazmín De Anda González, MD Franciscoc J. Gómez-Pérez, MD Daniel Cuevas-Ramos, MD |
author_sort |
César Ernesto Lam-Chung, MD |
title |
Acromegaly and a Giant Retroperitoneal Liposarcoma Producing IGF-1 |
title_short |
Acromegaly and a Giant Retroperitoneal Liposarcoma Producing IGF-1 |
title_full |
Acromegaly and a Giant Retroperitoneal Liposarcoma Producing IGF-1 |
title_fullStr |
Acromegaly and a Giant Retroperitoneal Liposarcoma Producing IGF-1 |
title_full_unstemmed |
Acromegaly and a Giant Retroperitoneal Liposarcoma Producing IGF-1 |
title_sort |
acromegaly and a giant retroperitoneal liposarcoma producing igf-1 |
publisher |
Elsevier |
series |
AACE Clinical Case Reports |
issn |
2376-0605 |
publishDate |
2020-07-01 |
description |
ABSTRACT: Objective: Liposarcoma is the most common histotype of retroperitoneal sarcomas, representing up to 45% of all cases. We report a rare combination of acromegaly and liposarcoma in the same individual. Methods: Laboratory and imaging studies including an oral glucose tolerance test, measurements of growth hormone (GH) and insulin-like growth factor-1 (IGF-1), and a computed tomography scan were performed. Results: The patient was a 60-year-old male with a history of acromegaly diagnosed on the basis of elevated IGF-1 at 1,373 ng/mL (age-appropriate reference range is 87 to 225 ng/mL) and macroadenoma treated with transsphenoidal surgery. He presented 8 years later with a history of abdominal distension and weight loss. Physical examination was notable for a right-sided abdominal mass that was tense and non-fluctuant. Two years earlier, he had a post oral glucose tolerance test GH level <0.25 ng/mL and IGF-1 level of 256 ng/mL (age-appropriate reference range is 55 to 206 ng/mL). Pituitary magnetic resonance imaging reported a 3.7 × 2.0-mm left-sided parasagittal lesion. Computed tomography scan showed a 25.0 × 22.0 × 32.3-cm heterogeneous giant mass in the right abdomen corresponding to a liposarcoma causing displacement of kidney, liver, and bowel loops. The patient was treated with a complete en bloc resection of the liposarcoma with the right kidney (45 × 33 × 17 cm) and tumor (9,400 g). Immunohistochemical examination revealed positive IGF-1 and GH staining. The patient suffered postoperative gastrointestinal bleeding that resulted in hemorrhagic shock and died on the 29th postoperative day after a cardiorespiratory arrest. Conclusion: Acromegalic patients are at increased risk of developing various types of neoplasms. This is the first documented coexistence of liposarcoma and history of acromegaly. |
url |
http://www.sciencedirect.com/science/article/pii/S2376060520300092 |
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