An Unusual Case of Gullo's Syndrome Concomitant with Serious Endometriosis Disease in a Postmenopausal Woman
This case describes a postmenopausal woman with severe endometriosis who presented with benign pancreatic hyperenzymemia (Gullo's syndrome) that persisted over five years without pancreatic pathology.
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This case report describes a 54-year-old postmenopausal woman with extensive, laparoscopically confirmed endometriosis and episodic abdominal complaints who was found on routine testing to have persistently elevated serum amylase and markedly increased lipase, with abnormal pancreatic isoamylase, but normal blood counts, chemistry, and tumor markers. After negative serologic workup for viral causes and negative testing for other common etiologies of hyperamylasemia/hyperlipasemia (including macroamylasemia, autoimmune disease, celiac disease, and inflammatory bowel), abdominal ultrasound and MRI repeatedly showed a normal pancreas, liver, and biliary tree, and the patient was followed for five years with fluctuating enzyme levels without symptoms or evidence of pancreatic pathology; the authors interpret this pattern as sporadic Gullo’s syndrome. A major limitation is the lack of repeat laparoscopy during follow-up to track the status and extent of her endometriosis implants, which prevents clarification of whether the two conditions are mechanistically linked versus coincidental. This paper is centrally about endometriosis — it reports Gullo’s syndrome occurring concomitantly with a history of severe endometriosis disease and discusses whether pancreatic enzyme hyperenzymemia could be related to endometriosis complications or may be coincidental.
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References (12)
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- Endometriosis: a premenopausal disease? Age pattern in 42,079 patients with endometriosis via openalex
- Extrapelvic endometriosis via openalex
- Extrapelvic Endometriosis via openalex
- Theories on the pathogenesis of endometriosis via openalex
- W2101742339 via openalex
- W2135108837 via openalex
- W2185293568 via openalex
- W2050386266 via openalex
- W1976597376 via openalex
- W2094995447 via openalex
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