| Issue | 
	Section | 
        Title | 
	File | 
											
				| Vol 17, No 3 (2018) | 
		LITERATURE REVIEW | 
		Morphological diagnosis and assessment of the malignant potential in pediatric adrenal cortical neoplasms | 
		
																		  (Rus)
														 | 
		
												
				| Vol 17, No 4 (2018) | 
		CLINICAL OBSERVATIONS | 
		Sinonasal renal cell-like adenocarcinoma | 
		
																		  (Rus)
														 | 
		
												
				| Vol 18, No 3 (2019) | 
		CLINICAL OBSERVATIONS | 
		Syndromе associated with multiple venous malformations (Bean syndrome) | 
		
																		  (Rus)
														 | 
		
												
				| Vol 19, No 2 (2020) | 
		CLINICAL OBSERVATIONS | 
		Atypical aggressive development of pigmented epithelioid melanocytoma in patient with Fanconi Anemia after hematopoietic stem cell transplantation | 
		
																		  (Rus)
														 | 
		
												
				| Vol 20, No 1 (2021) | 
		CLINICAL OBSERVATIONS | 
		Repidly involuting congenital hemangioma | 
		
																		  (Rus)
														 | 
		
												
				| Vol 20, No 1 (2021) | 
		LITERATURE REVIEW | 
		Infantile hemangioma explained in simple terms | 
		
																		  (Rus)
														 | 
		
												
				| Vol 20, No 3 (2021) | 
		ORIGINAL ARTICLES | 
		Kaposiform hemangioendothelioma/Kasabach–Merritt syndrome. Сlinical and laboratory characteristics. Analysis of clinical cases | 
		
																		  (Rus)
														 | 
		
												
				| Vol 20, No 4 (2021) | 
		CLINICAL OBSERVATIONS | 
		Giant cell angioblastoma | 
		
																		  (Rus)
														 | 
		
												
				| Vol 21, No 3 (2022) | 
		CLINICAL OBSERVATIONS | 
		Multifocal lymphangioendotheliomatosis with thrombocytopenia/cutaneovisceral angiomatosis with thrombocytopenia | 
		
																		  (Rus)
														 | 
		
												
				| Vol 22, No 2 (2023) | 
		CLINICAL OBSERVATIONS | 
		Kaposiform lymphangiomatosis with Kasabach–Merritt phenomenon | 
		
																		  (Rus)
														 | 
		
												
				| Vol 22, No 4 (2023) | 
		ORIGINAL ARTICLES | 
		Bilateral pheochromocytoma in patients with von Hippel–Lindau syndrome: clinical and molecular genetic features | 
		
																		  (Rus)
														 |