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Multisystemic Sarcoidosis Presenting with Widespread Vertebral Osseous and Visceral Lesions Masquerading as Metastatic Disease: A Case Report and Literature Review

Patient: Female, 78-year-old Final Diagnosis: Multisystem sarcoidosis with visceral and vertebral disease • sarcoidosis Symptoms: Weaknes of lower limbs Medication:— Clinical Procedure: — Specialty: Rheumatology OBJECTIVE: Rare disease BACKGROUND: Sarcoidosis is a systemic granulomatous disease whic...

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Detalles Bibliográficos
Autores principales: Saad, Eltaib, Agab, Mohamed, Zhang, Qishuo, Egoryan, Goar, Babkir, Akram, Filipiuk, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833267/
https://www.ncbi.nlm.nih.gov/pubmed/35125492
http://dx.doi.org/10.12659/AJCR.935158
Descripción
Sumario:Patient: Female, 78-year-old Final Diagnosis: Multisystem sarcoidosis with visceral and vertebral disease • sarcoidosis Symptoms: Weaknes of lower limbs Medication:— Clinical Procedure: — Specialty: Rheumatology OBJECTIVE: Rare disease BACKGROUND: Sarcoidosis is a systemic granulomatous disease which predominantly affects the lungs, skin, and lymph nodes. Vertebral sarcoidosis is a rare entity. The clinical presentation of sarcoidosis with diffuse vertebral osseous and visceral lesions, simulating a disseminated metastatic cancer, is extremely unusual and has been reported only in a handful of cases in the current literature. CASE REPORT: A 78-year-old White female patient with a remote history of asymptomatic pulmonary sarcoidosis presented with a 1-month history of generalized weakness. Physical examination was positive for upper and lower midline spinal tenderness. Laboratory findings showed anemia, hypercalcemia, and deranged liver functions. Abdominal imaging revealed an enlarged and nodular liver, ascites, splenomegaly, and enlarged retroperitoneal lymph nodes. Spinal imaging demonstrated several multi-level vertebral osseous lesions suspicious for metastatic bone cancer. Following extensive diagnostic work-up to rule out underlying metastatic cancers, a bone biopsy from an iliac lesion demonstrated active non-caseating granulomas, and a diagnosis of multisystemic sarcoidosis was made. The patient was started on systemic corticosteroids and demonstrated a gradual symptomatic improvement. Follow-up imaging revealed interval resolution of vertebral lesions. CONCLUSIONS: The clinical and radiological features of vertebral sarcoidosis can be indistinguishable from metastatic bone cancers. The possibility of widespread extrapulmonary sarcoidosis should be considered in any patients with a remote history of pulmonary sarcoidosis who experience simultaneous onset of unexplained multisystemic symptoms.