This article presents the case of a 22-year-old woman at 29 weeks of pregnancy, who exhibited recent onset neurologic symptoms including paresthesia of the right side of the face, involuntary myoclonic movements in the ipsilateral hand, 1 week of weakness in the right side of the body, and imaging features that were highly suggestive of a brain tumor diagnosis. A challenging decision making process was conducted by a team of multidisciplinary experts, leading to a consensus on adopting a conservative approach involving the use of steroids and antiepileptic medications, to which the patient responded favorably. When the patient reached 34 weeks of pregnancy, a cesarean section was performed, without complications, with the delivery of a healthy premature newborn. Upon delivery, surgical resection of the brain lesion was performed. Histopathologic analysis of the biopsy did not show signs consistent with neoplasia. Instead, it highlighted areas of necrosis along with the presence of granulomas and giant cells. Notably, despite extensive testing and staining for tuberculous bacilli across multiple samples yielding negative results, definitive confirmation was only secured via a gene X-pert test on the biopsied tissue. This diagnostic process emphasizes the importance of considering infectious diseases in atypical cases, highlighting the complexity of neurologic symptom assessment during pregnancy and the need to explore epidemiologic, systemic, and personal history factors.
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http://dx.doi.org/10.1002/ijgo.70045 | DOI Listing |
J Craniofac Surg
March 2025
Department of Oculoplastic Surgery, Beijing Tongren Eye Center, Beijing Tongren Hospital; Beijing Key Laboratory of Ophthalmology and Visual Sciences, Capital Medical University, Beijing, China.
Study Design: Retrospective, noncomparative, and interventional case series.
Objective: Peripunctal tumors are uncommonly encountered. The management at the aesthetically and functionally sensitive area is demanding.
Cureus
February 2025
Internal Medicine, The Queen's Medical Center, Honolulu, USA.
Lactic acidosis is an uncommon metabolic complication of malignancy, often associated with high tumor burden and increased mortality, and more frequently observed in hematologic malignancies than in solid tumors. This case report describes a patient with newly diagnosed signet ring cell carcinoma of the cecum, an uncommon and aggressive histological subtype of colon cancer, complicated by severe type B lactic acidosis. A 66-year-old female patient with primary signet ring cell carcinoma of the cecum and peritoneal carcinomatosis underwent a right colectomy with extended small bowel resection.
View Article and Find Full Text PDFInt J Surg Case Rep
March 2025
Department of Gynecology and Obstetrics, CHU Fattoma Bourguiba, University of Monastir, Tunisia.
Background And Importance: Placental site trophoblastic tumor (PSTT) a rare form of gestational trophoblastic disease, originates from intermediate trophoblastic cells and presents with nonspecific symptoms, complicating diagnosis. PSTT primarily affects women of childbearing age, but occurrences in perimenopausal women are exceptionally rare.
Case Presentation: We report a case of a 54-year-old perimenopausal woman presenting with a two-month history of abnormal uterine bleeding.
Indian J Otolaryngol Head Neck Surg
January 2025
Department of Otolaryngology, Command Hospital (EC), Kolkata, India.
Introduction: Neuroendocrine tumours of the larynx are extremely rare, though they make up only 1% of tumours in this region with the most common site being the supraglottis. On exhaustive research on PubMed, there are only a few prior cases of neuroendocrine carcinoma of subglottis published in the literature.
Case Report: A 56-year-old male presented to our center with complaints of hoarseness and dyspnoea for 1 month which was insidious in onset and gradually progressive.
Indian J Otolaryngol Head Neck Surg
February 2025
Dept. of Pathology, IMS and SUM Hospital, Bhubaneswar, India.
Isolated cystic cervical swelling may be a presentation of a branchial cyst, tubercular lymphadenitis, or maybe a metastatic lymphadenopathy from different head and neck subsites like pharynx and thyroid, etc. The location or level of swelling may give hints towards the primary pathology from where it spreads. Aspiration cytology and radiology sometimes fail to confirm its malignant nature and the primary site of origin.
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