Evidence map›Paper›PMID 41112428›Full record

ArticleNMC case report journal2025

Rapid Growth of a Lung Cancer Metastasis to a Pituitary Neuroendocrine Tumor: A Case Report and Literature Review.

Teppei Kawabata, Yasumasa Nishida, Takahiro Oyama, Tasuku Imai, Tomoyuki Noda, Shinji Mii, Naoko Inoshita, Hideki Maki

Abstract readCase Reports
In one paragraph

Article in NMC case report journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Teppei KawabataDepartment of Neurosurgery, Ogaki Municipal Hospital, Ogaki, Gifu, Japan.
Yasumasa NishidaDepartment of Neurosurgery, Ogaki Municipal Hospital, Ogaki, Gifu, Japan.
Takahiro OyamaDepartment of Neurosurgery, Ogaki Municipal Hospital, Ogaki, Gifu, Japan.
Tasuku ImaiDepartment of Neurosurgery, Ogaki Municipal Hospital, Ogaki, Gifu, Japan.
Tomoyuki NodaDepartment of Neurosurgery, Ogaki Municipal Hospital, Ogaki, Gifu, Japan.
Shinji MiiDepartment of Pathology, Ogaki Municipal Hospital, Ogaki, Gifu, Japan.
Naoko InoshitaDepartment of Pathology, Moriyama Memorial Hospital, Edogawa, Tokyo, Japan.
Hideki MakiDepartment of Neurosurgery, Ogaki Municipal Hospital, Ogaki, Gifu, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present an extremely rare case of lung cancer that metastasized to a gonadotroph pituitary neuroendocrine tumor, along with other organs. A 73-year-old man presented with dysarthria and bitemporal hemianopia. Head magnetic resonance imaging revealed cerebellar infarction and a pituitary tumor. Endoscopic transnasal pituitary tumor resection was performed. Pathologically, the tumor consisted of a well-differentiated neuroendocrine component, suggestive of a pituitary neuroendocrine tumor, alongside a poorly differentiated, highly malignant tumor with invasive growth. One month postoperatively, gadolinium-enhanced head magnetic resonance imaging revealed rapid growth of the residual tumor. Whole-body computed tomography and positron emission tomography revealed a 10-mm lung tumor and multiple muscle and bone metastases. Pathological examination of the pituitary tumor revealed poorly differentiated malignant cells. It was initially hypothesized that the pituitary neuroendocrine tumor had undergone malignant transformation with systemic metastases. However, further pathological examinations revealed steroidogenic factor 1-positive differentiated cells and steroidogenic factor 1-negative, synaptophysin-negative, cytokeratin-7-positive, and thyroid transcription factor-1-positive poorly differentiated malignant cells. The final diagnosis classified the tumor as a poorly differentiated lung adenocarcinoma that had metastasized to a gonadotroph pituitary neuroendocrine tumor, which showed rapid growth. Radiation and chemotherapy were administered; however, the patient died 6 months after surgery. Tumor metastasis to a pituitary neuroendocrine tumor is typically seen in older adults with non-functioning pituitary neuroendocrine tumors and no diabetes insipidus. Hence, clinicians should consider both metastatic pituitary neuroendocrine tumors and tumor metastasis to a pituitary neuroendocrine tumor when diagnosing a rapidly growing pituitary tumor in patients with signs of systemic metastasis.

Indexed as

collision tumorgonadotroph PitNETlung cancer

Identifiers

PMID41112428
PMCPMC12531372

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.