DOEGE-POTTER SYNDROME ARISING FROM AGGRESSIVE RECURRENT FIBROUS TUMOUR OF THE LUNG

INTRODUCTION Doege-Potter Syndrome (DPS) is a rare paraneoplastic syn- drome characterized by hypoinsulinemic hypoglycaemia. It typically arises in patients with mesenchymal tumours, particularly fibrous tumours of the lung. DPS is secondary to ectopic secretion of high-molecular-weight insulin-like growth factor (IGF)-2 that induces hypoglycemia. CASE We report a 56-year-old male with an underlying solitary fibrous lung tumour that was resected in 2013, which recurred in 2023 and was deemed unresectable. He was to undergo chemotherapy. However, while waiting, he presented neuroglycopenia with a capillary blood glucose of 1.9 mmol/L, reversed with glucose administration. Imaging studies revealed a large pleural-based lesion on the left with an interval increment in size, with its largest diameter at 20.6 cm and worsening mass effect. Histopathology report from CT-guided biopsy confirmed diagnosis of recurrent fibrous tumour with no malignant features. Renal and liver profiles were normal, and HbA1c was 4.3%. Paired random blood glucose was 2.8 mmol/L, with suppressed C-peptide and insulin levels of 31.81 pmol/L (NR 366.66-1466.65) and <1.39 pmol/L (NR 17.8- 173), respectively. Serum IGF-1 was normal at 166.2 ng/ml (NR 54.3-194.2). Serum IGF-2 was 479 ng/ml (NR 333-967), with an IGF-2:IGF-1 ratio of 3, supporting the diagnosis of IGF-2-mediated hypoglycemia. We started him with oral prednisolone 0.5 mg/kg/day, and the hypoglycaemia improved. Unfortunately, he succumbed to respiratory failure due to advanced tumour progression. Given the clinical findings and available biochemical markers, this case is consistent with a diagnosis of non-islet cell tumour hypoglycaemia (NICTH). CONCLUSION This case emphasizes the association between solitary fibrous tumours of the lung and DPS, highlighting the potential for recurrence of the tumour and persistent paraneoplastic effects. Early recognition and appropriate management of DPS are crucial in improving patient outcomes, such as the commencement of corticosteroids, while awaiting definitive treatment.

Authors

Publication Details

Journal
Journal of the ASEAN Federation of Endocrine Societies
Published
2025-05-30
DOI
https://doi.org/10.15605/jafes.040.s1.035
Primary Topic
Soft tissue tumor case studies
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

DOEGE-POTTER SYNDROME ARISING FROM AGGRESSIVE RECURRENT FIBROUS TUMOUR OF THE LUNG

Nadila Nur Azmi, Masliza Hanuni Mohd Ali, Siti Sanaa Wan Azman
Journal of the ASEAN Federation of Endocrine Societies
Soft tissue tumor case studies
article

DOEGE-POTTER SYNDROME ARISING FROM AGGRESSIVE RECURRENT FIBROUS TUMOUR OF THE LUNG

Nadila Nur Azmi, Masliza Hanuni Mohd Ali, Siti Sanaa Wan Azman
article en

Abstract

INTRODUCTION Doege-Potter Syndrome (DPS) is a rare paraneoplastic syn- drome characterized by hypoinsulinemic hypoglycaemia. It typically arises in patients with mesenchymal tumours, particularly fibrous tumours of the lung. DPS is secondary to ectopic secretion of high-molecular-weight insulin-like growth factor (IGF)-2 that induces hypoglycemia. CASE We report a 56-year-old male with an underlying solitary fibrous lung tumour that was resected in 2013, which recurred in 2023 and was deemed unresectable. He was to undergo chemotherapy. However, while waiting, he presented neuroglycopenia with a capillary blood glucose of 1.9 mmol/L, reversed with glucose administration. Imaging studies revealed a large pleural-based lesion on the left with an interval increment in size, with its largest diameter at 20.6 cm and worsening mass effect. Histopathology report from CT-guided biopsy confirmed diagnosis of recurrent fibrous tumour with no malignant features. Renal and liver profiles were normal, and HbA1c was 4.3%. Paired random blood glucose was 2.8 mmol/L, with suppressed C-peptide and insulin levels of 31.81 pmol/L (NR 366.66-1466.65) and <1.39 pmol/L (NR 17.8- 173), respectively. Serum IGF-1 was normal at 166.2 ng/ml (NR 54.3-194.2). Serum IGF-2 was 479 ng/ml (NR 333-967), with an IGF-2:IGF-1 ratio of 3, supporting the diagnosis of IGF-2-mediated hypoglycemia. We started him with oral prednisolone 0.5 mg/kg/day, and the hypoglycaemia improved. Unfortunately, he succumbed to respiratory failure due to advanced tumour progression. Given the clinical findings and available biochemical markers, this case is consistent with a diagnosis of non-islet cell tumour hypoglycaemia (NICTH). CONCLUSION This case emphasizes the association between solitary fibrous tumours of the lung and DPS, highlighting the potential for recurrence of the tumour and persistent paraneoplastic effects. Early recognition and appropriate management of DPS are crucial in improving patient outcomes, such as the commencement of corticosteroids, while awaiting definitive treatment.

Journal of the ASEAN Federation of Endocrine SocietiesVol. 40(S1)
Openalex Percentile: Top 81%
Soft tissue tumor case studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

DOEGE-POTTER SYNDROME ARISING FROM AGGRESSIVE RECURRENT FIBROUS TUMOUR OF THE LUNG — Nadila Nur Azmi, Masliza Hanuni Mohd Ali, et al. · Journal of the ASEAN Federation of Endocrine Societies (2025) | TGRS Research Map | TGRS