A 69-year-old white male patient with a past medical history of hypertension, coronary artery disease with prior stents, atrial fibrillation status post ablation, and a recent diagnosis of pheochromocytoma presented with hypertensive urgency in the setting of intense nausea and vomiting. A month and a half prior, pheochromocytoma was diagnosed during atrial fibrillation ablation, when he experienced periprocedural hypertensive emergency with systolic blood pressures > 250 mmHg, flash pulmonary edema, and hemoptysis. A computed tomography (CT) chest scan, ordered for hemoptysis, incidentally demonstrated an 8.5 × 7.5 × 7.2 cm left adrenal mass. Further history uncovered several years of intermittent pounding headaches, diaphoresis, nausea, and palpitations. Biochemical studies revealed total urine metanephrines elevated to 8193 mcg/24 hour (normal range 233–716) with elevations in both urinary metanephrines to 2909 mcg/24 hour (normal range 44–261) and normetanephrine to 5284 mcg/24 hour (normal range 138–521). Pulmonary edema and hypoxia resolved with diuresis. He was started on doxazosin 4 mg per os daily with close blood pressure monitoring, anticipating surgical adrenalectomy in approximately 6 weeks.

Our patient was asymptomatic after discharge until 2 days before scheduled surgery, when he developed worsening periumbilical pain, rated 4 out of 10 in severity, with nausea and vomiting. He reported ten episodes of emesis with repeated, severe retching over 12 hours prior to presentation to the emergency room. He denied headache, diarrhea, bloody stool, flank pain, hematuria, chest pain, shortness of breath, palpitations, diaphoresis, fever, chills, any recent changes to his diet, or sick contacts. His wife did not experience similar symptoms. He recalled similar emetic episodes over the last few years that resolved without medical intervention.

In the emergency department, his initial blood pressure was 201/113 mmHg with a heart rate in the 80s. His baseline blood pressure, with alpha adrenergic blockade, was a mean arterial pressure (MAP) between 80 mmHg and 100 mmHg (Fig. 1). He was afebrile with a room air oxygen saturation of 98% and an unremarkable physical exam. His abdomen was soft, nontender, nondistended, with normo-active bowel sounds in all four quadrants and negative for peritoneal signs, such as guarding or rebound tenderness.

Laboratory tests were unremarkable and without evidence of end-organ damage. His white blood cell count was 6.6 K/ul, with a normal hemoglobin, and mild thrombocytopenia at 119 K/ul. Electrolytes, creatinine, liver enzymes, lipase, lactate, and troponin I were all normal. Urinalysis showed a urine specific gravity of > 1.060 with 1 + ketones and protein, without blood, positive nitrites, or leukocyte esterase. Urine toxicology screen was positive for tetrahydrocannabinol (THC).

A CT abdomen and pelvis with intravenous contrast redemonstrated left adrenal mass measuring 7.1 × 8.7 × 7.1 cm, as well as diffuse diverticulosis without evidence of acute abnormalities.

The patient reported many years of frequent cannabis use. A year and half prior to presentation, he began using 87–88% THC with cannabidiol (CBD) in a smoke pen, taking 5–6 “hits” per day. Prior to that, he would smoke about 2–3 cannabis “joints” per day but denied ever eating cannabis. He also endorsed using chewing tobacco consistently over the last 30 years, using one can of tobacco over 4–6 days. He denied smoking tobacco, other recreational drugs, or alcohol.

Our patient had no evidence of new abdominal pathology or end-organ damage, ruling out pheochromocytoma multisystem crisis as a cause for his hypertension or gastrointestinal symptoms. Given that his blood pressure was well controlled prior to this episode, it was hypothesized that his hypertension was likely secondary to physical abdominal compression of his large adrenal tumor from forceful retching, leading to a release of catecholamines. Later, during surgical adrenalectomy under general anesthesia, a hypertensive event coincided with gas insufflation of the abdomen to 15 mmHg, an indirect affirmation of this hypothesis (Fig. 2). His large tumor also made it more likely that elevated abdominal pressure during retching could release catecholamines. Our initial differential diagnosis included ischemic bowel, cholecystitis, gastroenteritis, and CHS, but lab values and abdominal CT scan did not reveal any acute intraabdominal process that could explain his severe nausea and emesis. It should be noted that no evidence of intestinal ischemia was found that might have been a cause of nausea and vomiting. As the patient denied any sick contacts and his wife remained asymptomatic despite consuming the same food items, the diagnosis of viral or bacterial gastroenteritis became less likely. Noncompliance leading to poor blood pressure control was also considered, however, the patient was diligent in reporting blood pressures measured at home and confirming medication doses with regular emails to one of the authors. Upon eliciting the patient’s long history of recurring vomiting episodes and long-standing, frequent cannabis use, the diagnosis of CHS was the most likely explanation.

The patient was given intravenous phentolamine 5 mg, intravenous lorazepam 0.5 mg, and a lactated Ringer’s fluid bolus with improvement of his nausea. He was subsequently admitted to the medical intensive care unit (MICU) for close blood pressure monitoring and titration.

In the MICU, he required three doses of intravenous ondansetron 4 mg and one dose of intravenous lorazepam 0.25 mg for further nausea management. He was started on a clevidipine infusion, in addition to his home dose of per os doxazosin 4 mg daily for a MAP goal of less than 100 mmHg. Given that the patient’s MAP remained slightly elevated despite clevidipine and doxazosin, he was started on per os phenoxybenzamine 10 mg daily, which he tolerated well. By hospital day 2, the patient’s retching and vomiting stopped, and his diet was advanced. He was eventually weaned off clevidipine with per os doxazosin 6 mg/day and per os phenoxybenzamine 20 mg/day and discharged with the recommendation to stop cannabis and tobacco use.

Follow-up 1 week after discharge showed normalization of his blood pressure with no recurrence of his gastrointestinal symptoms (Fig. 1). He underwent successful adrenalectomy 2 weeks after discharge.