Rodriguez Vania, Sridhar Ramya, Manzano Alex, Al Sabbagh Aliaa, Howard Lydia, Baker Paul, Mauyra Preetika
Mount Sinai Medical Center, Miami Beach, FL, USA.
Command Hospital, Lucknow, India.
J Investig Med High Impact Case Rep. 2025 Jan-Dec;13:23247096251358668. doi: 10.1177/23247096251358668. Epub 2025 Jul 18.
Giant pheochromocytomas are rare tumors, typically exceeding 7 cm in size. Most are noncatecholamine secreting due to tumor necrosis and connective tissue content. Their presentation can range from classic hyperadrenergic symptoms to vague gastrointestinal complaints. Larger tumors are associated with higher risks of metastasis, mortality, and perioperative complications. Our case presents a 31-year-old female who presented with the chief complaint of vomiting, associated with intermittent palpitations and elevated blood pressure, with subsequent imaging revealing an 8.7 cm right adrenal mass. Complete resection of the mass showed a 10 × 7 × 3.9 cm mass that occupied the entire adrenal medulla, consistent with a giant pheochromocytoma. This case contributes to the evidence supporting a minimally invasive approach as well as individualized management of giant pheochromocytomas. Furthermore, it emphasizes the importance of a high clinical suspicion in the context of vague symptoms.
巨大嗜铬细胞瘤是罕见肿瘤,通常大小超过7厘米。由于肿瘤坏死和结缔组织成分,大多数肿瘤不分泌儿茶酚胺。其临床表现范围可从典型的高肾上腺素能症状到模糊的胃肠道不适。较大的肿瘤与转移、死亡及围手术期并发症的风险更高相关。我们的病例是一名31岁女性,主要症状为呕吐,伴有间歇性心悸和血压升高,随后影像学检查发现右侧肾上腺有一个8.7厘米的肿块。肿块完整切除后显示为一个10×7×3.9厘米的肿块,占据整个肾上腺髓质,符合巨大嗜铬细胞瘤。该病例为支持巨大嗜铬细胞瘤的微创方法及个体化管理提供了证据。此外,它强调了在症状模糊的情况下保持高度临床怀疑的重要性。